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Published med-spa & injectable compliance alerts · monitoring, not legal advice
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Border enforcement · last 90 days
FDA Import Refusals · counts of published records
FDA refused 201 shipments of unapproved or violative injectables at the U.S. border from 111 firms across 22 countries — the gray-market corridor to source away from.
| Product class | Shipments | Firms | Countries |
|---|---|---|---|
| Dermal fillersincl. QUIVER MEDIC INC., Q-Med AB, Daehan Nupharm | 114 | 71 | 18 |
| Botulinum toxinincl. Medytox Inc., Allergan Pharmaceuticals Ireland, COMEM NATURAL JSC | 52 | 21 | 7 |
| GLP-1 drugsincl. ELI LILLY JAPAN, TANDJIGORA MOHAMED, Eli Lilly Italia SPA | 21 | 14 | 10 |
| Injectable anestheticsincl. BIOPHARMA, Daehan Nupharm, SANKALP HEALTHCARE | 14 | 14 | 8 |
Source: FDA Data Dashboard import refusals. A refusal is a border action, not a finding against any U.S. practice. Named firms are the foreign shippers/manufacturers on FDA’s record.
Showing everything, including routine background items (bulk import refusals, inspection citations).
Show material only →- CAUTIONWIScope of PracticeSep 21, 2026
WI State Administrative Register: 849A3 Register (9/21/2026) - 2026-09-21
Wisconsin Board of Nursing emergency rules affecting APRNs.
What to do — members only.Become a member →State Administrative Registerprimary source ↗ - MONITORFEDMulti-topicSep 21, 2026
Primary Source Monitoring: Former Connecticut Resident Guilty of Operating Websites to Illegally Sell Misbranded and Unapproved Drugs
Caution urged due to recent conviction for selling misbranded drugs.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDDermal FillersSep 17, 2026
Primary Source Monitoring: Korea Filler Experts - 718706 - 11/03/2025
FDA warns koreafillerexperts.com over unapproved, misbranded injectable botulinum toxin.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refused entry of ONABOTULINUMTOXINA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Numeco · Unknown · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses shipment of collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · MAYPHARM · Geumcheon · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Lidocaine (South Korea)
Lidocaine from South Korea was refused entry by the FDA; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daehan Nupharm · Hwaseong · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAISep 16, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Ireland)
FDA refuses entry of OnabotulinumtoxinA from Ireland.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Pharmaceuticals Ireland · Westport · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry of OnabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Inc. · Cheongju · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Lidocaine (South Korea)
FDA refuses lidocaine shipment from South Korea due to violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · BIOPHARMA · Seoul · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of South Korean dermal collagen implants.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · QUIVER MEDIC INC. · Yeongdeungpo · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDGLP-1 CompoundingSep 16, 2026
Primary Source Monitoring: FDA clarifies policies for compounders as national GLP-1 supply begins to stabilize
FDA updates compounding guidelines as GLP-1 supplies stabilize.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refused a shipment of collagen implants from Sweden — avoid gray-market sour
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of South Korean collagen implants for aesthetics.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daehan Nupharm · Hwaseong · plastic-surgery device · refused as misbranding, adulteration
- CRITICALFEDAesthetic DevicesSep 16, 2026
FDA device recall (Class II): Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy a…
FDA recalls DermaV Laser System; check for safety compliance.
What to do — members only.Become a member →FDA Device Recallprimary source ↗ - MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Vietnam)
FDA refuses ONABOTULINUMTOXINA from Vietnam; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · COMEM NATURAL JSC · Ha Noi · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAISep 16, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA rejects ONABOTULINUMTOXINA shipment from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daewoong Pharmaceutical Co. Ltd. (Hyangnam factory) · Hwaseong · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Daxxify (daxibotulinumtoxinA)-LANM (Vietnam)
FDA blocks import of DaxibotulinumtoxinA-Lanm from Vietnam.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · COMEM NATURAL JSC · Ha Noi · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAISep 16, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses shipment of dermal collagen from France — verify your sources.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Industrie SAS · Pringy · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesSep 16, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry for South Korean dermal collagen implants.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Pharmaresearch · Gangneung-si · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDGLP-1 CompoundingSep 15, 2026
Primary Source Monitoring: Hefner v. Rock Valley Compounding Pharmacy, LLC (3:26-cv-01298) — District Court, S.D. Illinois
Legal case filed affecting compounding pharmacy standards.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesSep 15, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses shipment of dermal collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · KORESTETICS · Incheon Yeon · plastic-surgery device · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesSep 15, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Canada)
FDA refuses entry of Canadian dermal collagen shipment.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Prollenium Medical Technologies Inc. · Richmond Hill · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesSep 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Vietnam)
FDA refuses entry of collagen implant shipment from Vietnam.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · COMEM NATURAL JSC · Ha Noi · plastic-surgery device · refused as misbranding, adulteration, unapproved new drug
- MONITORFEDAesthetic InjectablesSep 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refused entry of a dermal collagen implant from Sweden on Sep 14, 2026.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused as misbranding
- CAUTIONWIScope of PracticeSep 14, 2026
WI State Administrative Register: 849A2 Register (9/14/2026) - 2026-09-14
Emergency rule from Wisconsin Board of Nursing may impact injectors.
What to do — members only.Become a member →State Administrative Registerprimary source ↗ - MONITORFEDAesthetic InjectablesSep 10, 2026
FDA import refusal: Lidocaine (India)
Lidocaine from India refused by FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · SANKALP HEALTHCARE · MAHARASTRA · drug product · refused as unapproved new drug
- MONITORFEDGLP-1 CompoundingSep 10, 2026
FDA import refusal: Tirzepatide (Anti-diabetic) (Japan)
FDA refuses tirzepatide import from Japan; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ELI LILLY JAPAN · Kobe · drug product · refused as unapproved new drug
- MONITORFEDGLP-1 CompoundingSep 9, 2026
Primary Source Monitoring: Human Drug Compounding Policies and Rules
FDA's compounding policy index adds a September 2026 neonatal nutrition guidance.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesSep 9, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry for OnabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Inc. · Cheongju · drug product · refused as unapproved new drug
- MONITORFEDGLP-1 CompoundingSep 9, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (France)
FDA refuses entry of French semaglutide shipment.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · TANDJIGORA MOHAMED · Aulnay Sous Bois · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesSep 8, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Spain)
FDA refused dermal collagen implants from Spain; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · SESDERMA SL · Pucol · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAISep 8, 2026
FDA import refusal: Daxxify (daxibotulinumtoxinA)-LANM
FDA refuses entry of DaxibotulinumtoxinA-Lanm from California.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Revance Therapeutics, Inc · Newark · drug product · refused as misbranding
- MONITORFEDGLP-1 CompoundingFDA: VAISep 8, 2026
FDA import refusal: Tirzepatide (Anti-diabetic) (Italy)
FDA refuses tirzepatide from Italy; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Eli Lilly Italia SPA · Sesto Fiorentino · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesSep 8, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses entry of collagen implants from France - verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · COTE DAZUR PHARMACY · Nice · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesSep 8, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refuses entry of dermal collagen implants from Sweden.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Jonas Lindgren, M.D. · Uppsala · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesSep 8, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry for collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Bio Plus Co. Ltd · Seongnam · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDGLP-1 CompoundingSep 4, 2026
Primary Source Monitoring: Eli Lilly v. Instant Rx (E.D.N.Y.) — Consent Judgment and Permanent Injunction as to defendants Dispensing Physician Consultants, Inc. d/b/a Ira's Di…
Injunction against suppliers may impact GLP-1 access for med spas.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDMulti-topicSep 4, 2026
Primary Source Monitoring: Med Spa Owner Sentenced to 46 Months in Prison for Performing Thousands of Counterfeit Botox and Filler Injections
Med spa owner sentenced for using counterfeit Botox and fillers.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesSep 3, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA blocks shipment of aesthetic collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · S THEPHARM CO · Uiwang-si · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesSep 3, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Switzerland)
FDA refuses entry for aesthetic collagen implants from Switzerland.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · PROFESSIONAL DERMA SA · Lugand · plastic-surgery device · refused as adulteration
- MONITORFEDAesthetic InjectablesSep 3, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Austria)
FDA rejects dermal collagen implant from Austria—verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · GALDERMA AUSTRIA GMBH · Vienna · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesSep 3, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of collagen implants from South Korea—verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · UNKNOWN · UNKNOWN · plastic-surgery device · refused as adulteration
- MONITORFEDAesthetic InjectablesSep 3, 2026
FDA import refusal: Implant, Dermal, for Aesthetic Use in the Hands (Sweden)
FDA refuses entry of dermal implants from Sweden.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesSep 3, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refused entry of collagen injectables from Sweden; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused entry by FDA
- MONITORFEDGLP-1 CompoundingSep 3, 2026
FDA import refusal: Tirzepatide (Anti-diabetic) (Japan)
FDA refuses tirzepatide entry from Japan; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Eli Lilly Japan K.K.Seishin Laboratories · Nishigun · drug product · refused as misbranding, unapproved new drug
- MONITORWAScope of PracticeSep 3, 2026
WA State Health Agency: Registered Nurse (RN) and Licensed Practical Nurse (Lpn) Licensing Requirements
RN and LPN licensing rules in Washington may affect aesthetic practices.
What to do — members only.Become a member →State Health Agencyprimary source ↗ - MONITORFEDAesthetic InjectablesSep 1, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refused a dermal collagen implant shipment from Sweden.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused as misbranding
- MONITORFEDPeptidesSep 1, 2026
Primary Source Monitoring: Peak Performance Peptides - 735127 - 08/24/2026
FDA warns about unapproved peptide products; assess your suppliers.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 31, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (Canada)
FDA refuses semaglutide shipment from Canada; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · NOVO NORDISK · Mississauga · drug product · refused entry by FDA
- MONITORFEDGLP-1 CompoundingAug 31, 2026
FDA import refusal: Tirzepatide (Anti-diabetic)
FDA blocks tirzepatide shipment from Indiana; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Eli Lillyand Company · Indianapolis · drug product · refused as unapproved new drug
- CAUTIONWIScope of PracticeAug 31, 2026
WI State Administrative Register: 848B Register (8/31/2026) - 2026-08-31
Wisconsin updates may alter scope-of-practice for injectors.
What to do — members only.Become a member →State Administrative Registerprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 28, 2026
Primary Source Monitoring: Agency Information Collection Activities; Proposals, Submissions, and Approvals: Registration of Human Drug Compounding Outsourcing Facilities Under …
FDA proposals may impact compounding practices for med spas.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - CAUTIONWIScope of PracticeAug 28, 2026
WI State Administrative Register: Register 848 - Inserted Chapter Sps 382 - 2026-08-28
Supervision standards for aesthetic practices in Wisconsin.
What to do — members only.Become a member →State Administrative Registerprimary source ↗ - CAUTIONWIScope of PracticeAug 28, 2026
WI State Administrative Register: Register 848 - Removed Chapter Sps 382 - 2026-08-28
Key supervision standards for med spas may have changed.
What to do — members only.Become a member →State Administrative Registerprimary source ↗ - CAUTIONOHLasers/EnergyAug 26, 2026
OH HB377: Regards use of light-based medical devices for hair removal
Ohio HB 377 sets supervision rules for light-based hair removal.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDAesthetic InjectablesFDA: VAIAug 26, 2026
FDA import refusal: Lidocaine (China)
FDA refused lidocaine import from Anhui, China; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Planet (Anhui) Pharmaceuticals Co., Ltd · Chuzhou · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 25, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (United Kingdom)
FDA refuses entry of UK collagen dermal implants — confirm violation details.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · MERZ PHARMA · Hemel Hempstead · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 25, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Switzerland)
Collagen implants from Switzerland refused entry by FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · PROFESSIONAL DERMA SA · Lugand · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 25, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry for onabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Inc. · Cheongju · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 25, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Switzerland)
FDA refuses entry of Swiss collagen implants — beware sourcing risks.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · MATEXLAB SA · Geneva · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 25, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refused entry of collagen implants from Sweden.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 25, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Switzerland)
FDA denies entry of Swiss collagen implants due to violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Teoxane S.A. · Geneva · plastic-surgery device · refused entry by FDA
- MONITORFEDMulti-topicAug 25, 2026
Primary Source Monitoring: Drug Shortages | Additional News and Information
Stay informed about updated drug shortages affecting aesthetics.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesAug 25, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry of OnabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · DAEWOONG PHARM CO LTD · Seoul · drug product · refused entry by FDA
- CAUTIONFEDAesthetic DevicesFDA: VAIAug 25, 2026
FDA Warning Letter: Advance-Esthetic LLC (Devices)
FDA says Zemits CrystalFrax Pro, Abigon Pro and Bionexis Lite Pro RF and light body-contouring devices lack required FDA approval or clearance.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - MONITORFEDMulti-topicAug 25, 2026
Primary Source Monitoring: Human Drug Compounding Outsourcing Facility Fees
FDA fees for drug compounding could affect your practice costs.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - CAUTIONFEDGLP-1 CompoundingAug 24, 2026
FDA Warning Letter: Peptide Partners, LLC (Drugs)
FDA says Peptide Partners' "research use only" GLP-1s and other injectable peptides are unapproved drugs. Health claims on its own product pages were FDA's evidence that they were intended for human use.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - CAUTIONFEDGLP-1 CompoundingAug 24, 2026
FDA Warning Letter: Royal Peptides LLC (Drugs)
FDA says Royal Peptides' "research use only" GLP-1s and other peptides are unapproved drugs. Its weight-loss claims, and the bacteriostatic water, "peptide guide" and "peptide calculator" sold alongside them, were FDA's evidence they were meant for injection in people.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - CAUTIONFEDGLP-1 CompoundingAug 24, 2026
FDA Warning Letter: Peak Performance Peptides (Drugs)
FDA says Peak Performance Peptides' "research use only" semaglutide, retatrutide and other peptides, and the BAC water sold with them, are unapproved.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - MONITORFEDAesthetic InjectablesFDA: VAIAug 23, 2026
FDA import refusal: Lidocaine (Anesthetic) (Canada)
Lidocaine from Canada refused entry by FDA – confirm violation details.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · HK Kolmar Canada, Inc. · Barrie · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 22, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refused entry for collagen implants from France; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · CHRISTIAN DIOR · Saint-Jean-De-Braye · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDMulti-topicAug 21, 2026
Primary Source Monitoring: Compounding Information for States
FDA issues new compounding guidance; check for local implications.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesAug 21, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses aesthetic collagen implants from South Korea; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · BioPlus Co.,Ltd. · Seongnam · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 21, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA blocks entry of onabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Co. Ltd. · Heungdeok-Gu · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesAug 21, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry of OnabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Huons Global Co. Ltd · Jecheon-Si · drug product · refused as unapproved new drug
- MONITORFEDMulti-topicAug 21, 2026
Primary Source Monitoring: Compounding and the FDA: Questions and Answers
FDA guidance on compounding released; impact on med spas unclear.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesAug 20, 2026
FDA import refusal: Acid, Hyaluronic, Intraarticular (Ireland)
FDA refused hyaluronic acid import from Ireland; confirm violation details.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · MYLAN INTERNATIONAL · Galway · medical device · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: VAIAug 19, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses ONABOTULINUMTOXINA from South Korea - verify your sources.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daewoong Pharmaceutical Co. Ltd. (Hyangnam factory) · Hwaseong · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIAug 19, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use
FDA refused entry of collagen dermal implants from Wisconsin.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Merz North America, Inc. · Franksville · plastic-surgery device · refused entry by FDA
- CRITICALFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, Apollo care, …
Recall of semaglutide from Apollo Care due to contamination risk.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Onl…
Recall of compounded semaglutide due to contamination reported.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injectio…
FDA recalls semaglutide 7.5mg due to particulate contamination.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, Apollo care, 3801 …
Recall of contaminated semaglutide vials.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, Apollo care, 380…
FDA recalls semaglutide 12.5mg due to contamination risks.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injecti…
Apollo Care recalls semaglutide for harmful particulate matter.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection On…
FDA recalls semaglutide due to contamination risks.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, Apollo care, 380…
FDA recalls semaglutide from Apollo Care due to contamination.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection On…
Important recall: Check your inventory for affected semaglutide vials.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA import refusal: Tirzepatide (Anti-diabetic) (Japan)
FDA refuses tirzepatide entry from Japan.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · MITSUBISHI TANABE PHARMA CORPORATION . · Osaka · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesAug 19, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses entry of dermal collagen implants from France.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · LABORATOIRES VIVACY · Paris-L'Hopital · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 19, 2026
FDA import refusal: Hyaluronidase (France)
FDA rejects hyaluronidase from France; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · IBSA Pharma SAS · Antibes · drug product · refused as misbranding, unapproved new drug
- MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, Apollo care, 380…
FDA recalls semaglutide vials due to contamination concerns.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 19, 2026
FDA recall (Class II): Semaglutide 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, Apollo care, …
FDA recalls semaglutide due to contamination risks.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDAesthetic InjectablesAug 19, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refused an injectable collagen shipment from Sweden; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused entry by FDA
- MONITORFEDGLP-1 CompoundingFDA: VAIAug 18, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (Denmark)
Semaglutide shipment from Denmark refused by FDA; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Novo Nordisk A/S · Bagsvard · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesAug 18, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA rejects collagen implant shipment from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q MED AB, SEMINARIEGATAN 21 · Gangwon · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesAug 18, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
OnabotulinumtoxinA shipment refused by FDA; check your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Inc. · Cheongju · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIAug 18, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Ireland)
FDA refuses entry to OnabotulinumtoxinA from Ireland — verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Pharmaceuticals Ireland · Westport · drug product · refused as misbranding, unapproved new drug · FDA lab-analyzed
- MONITORFEDGLP-1 CompoundingAug 17, 2026
Primary Source Monitoring: Illinois Man Charged With Scheme To Impersonate Doctors And Make False Statements To Obtain GLP-1 Medications
Fraud case underlines risks in GLP-1 medication practices.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Acid, Hyaluronic, Intraarticular (South Korea)
FDA refused entry of a hyaluronic acid shipment from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Across Co., Ltd · Chuncheon-si · medical device · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIAug 14, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (United Kingdom)
FDA refused onabotulinumtoxinA from Clwyd, UK; avoid overseas sources.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Ipsen BioPharm Ltd · Wrexham · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Japan)
FDA rejects collagen implants from Japan; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · TSK LABORATORY INTERNATIONAL, JAPAN · Tochigi · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry of onabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Inc. · Cheongju · drug product · refused as misbranding, unapproved new drug
- MONITORFEDGLP-1 CompoundingFDA: VAIAug 14, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (Denmark)
Semaglutide shipment from Denmark refused by FDA; verify your supplies.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Novo Nordisk A/S · Bagsvard · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIAug 14, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refused entry of OnabotulinumtoxinA from South Korea—avoid gray markets.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daewoong Pharmaceutical Co. Ltd. (Hyangnam factory) · Hwaseong · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIAug 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Switzerland)
FDA refuses entry of collagen products from Switzerland; verify sources.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · IBSA Institut Biochimique SA · Pazzallo · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refused entry of a collagen implant shipment from France.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Galderma Internati · La Defence Ce · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refused a shipment of South Korean collagen implants.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Across Co., Ltd · Chuncheon-si · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of collagen implant from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Janytree Inc. · Geumcheon · plastic-surgery device · refused as adulteration, misbranding
- MONITORFEDGLP-1 CompoundingAug 14, 2026
FDA import refusal: Tirzepatide (Anti-diabetic)
Tirzepatide from India refused entry by FDA; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Eli Lilly & Company · Indianapolis · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses entry for dermal collagen implants from France.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · LABORTORIES FILLMED · Paris-L'Hopital · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Lidocaine (Anesthetic) (South Korea)
FDA refuses lidocaine shipment from South Korea; supplier verification needed.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · GDK Cosmetics Co., Ltd. · Namdong · drug product · refused as adulteration
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA rejects collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Reanzen Co., Ltd · Pyeongtaek · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
Imports of collagen implants from South Korea denied by FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Koru Pharmaceuticals Co., Ltd · Gangnam · plastic-surgery device · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refused onabotulinumtoxinA from South Korea; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daewoong Pharmaceutical · Hwasung Gun · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Italy)
FDA refuses dermal collagen implant shipment from Italy.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · LICOFARMA SRL · Galatina · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: VAIAug 14, 2026
FDA import refusal: Lidocaine Hcl (Anesthetic) (France)
FDA refuses entry of Lidocaine HCl from France - verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Septodont Ou Septodont SAS Ou Specialites Septodont · St Maur Des Fosses · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesAug 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refused entry of dermal collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Genoss Co., Ltd · Suwon · plastic-surgery device · refused as misbranding
- MONITORFEDGLP-1 CompoundingFDA: VAIAug 13, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (Denmark)
Semaglutide shipment from Denmark refused by FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Novo Nordisk A/S · Bagsvard · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refused a shipment of collagen implants from France.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Industrie SAS · Pringy · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesFDA: VAIAug 13, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refused entry of OnabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daewoong Pharmaceutical Co. Ltd. (Hyangnam factory) · Hwaseong · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use
FDA refuses entry of collagen dermal implants from Missouri.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ELTA MD · Carrolton · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Italy)
FDA refuses collagen implant from Italy.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · IBSA Farmaceutici Italia Srl · Lodi · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refused collagen implants from Sweden; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
Dermal collagen implants from South Korea refused entry by the FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Feel Tech Co., Ltd · Jeonbuk · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
US FDA refused entry of dermal collagen from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Across Co., Ltd · Chuncheon-si · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Dermal Cooling PACK/VACUUM/MASSAGER (China)
FDA refuses entry of dermal products from China; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · SHENZHEN JINSHANG ELECTRONIC TEC · Shenzhen · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
OnabotulinumtoxinA from South Korea refused entry by FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · DAEWOONG PHARM CO LTD · Seoul · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: VAIAug 13, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Germany)
FDA refused entry of OnabotulinumtoxinA from Germany; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Merz Pharma Gmbh & Co. KGaA · Reinheim · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of dermal collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · BioPlus Co.,Ltd. · Seongnam · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
Import of collagen implants from South Korea refused by FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Inc. · Cheongju · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: VAIAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Canada)
FDA refused entry of Canadian collagen implants; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Prollenium Medical Technologies Inc. · Aurora · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry for collagen dermal implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Forest Hills Lab Korea Co Ltd · Gyeonggi-do · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses shipment of collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · DONGBANG MEDICAL CO.,LTD · Yongin-Si · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: VAIAug 13, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Ireland)
FDA blocks ONABOTULINUMTOXINA from Co. MAYO, Ireland.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Pharmaceuticals Ireland · Westport · drug product · refused as misbranding, unapproved new drug · FDA lab-analyzed
- MONITORFEDAesthetic InjectablesAug 13, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA denies entry of a collagen implant from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · PHARMARESEARCH CO., LTD. · Seongnam · plastic-surgery device · refused as misbranding
- MONITORFEDGLP-1 CompoundingFDA: VAIAug 12, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (Denmark)
FDA refused entry for semaglutide from Denmark.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Novo Nordisk A/S · Bagsvard · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesAug 12, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Vietnam)
FDA refused entry for Vietnamese collagen implants; verify your sources.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · NGUYEN VIET ANH - CCCD#035094002294 · Hanoi Center · plastic-surgery device · refused entry by FDA
- MONITORFEDPeptidesAug 12, 2026
Primary Source Monitoring: Eli Lilly and Company v. Lone Star Peptide Co. LLC (4:26-cv-06562) — District Court, S.D. Texas
Eli Lilly's lawsuit may impact peptide supply chains for med spas.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesAug 12, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refused collagen implant shipment from Sweden; verify your supplier.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIAug 12, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Canada)
FDA refuses collagen implant shipment from Canada; check your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Prollenium Medical Technologies Inc. · Aurora · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesAug 12, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Germany)
FDA refuses entry of OnabotulinumtoxinA from Hassia, Germany.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Merz Pharmaceuticals GmbH · Frankfurt Am Main · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 12, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Switzerland)
FDA refuses entry of Swiss collagen implants; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Teoxane S.A. · Geneva · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 12, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Vietnam)
FDA denied entry of ONABOTULINUMTOXINA from Vietnam due to violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · NGUYEN VIET ANH - CCCD#035094002294 · Hanoi Center · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 12, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses shipment of collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Dongbang Medical Co. Ltd · Dongbangbaekjungang-ro · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIAug 12, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (United Kingdom)
FDA refuses import of onabotulinumtoxinA from UK.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Ipsen BioPharm Ltd · Wrexham · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIAug 11, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refused entry of collagen implants from South Korea—check your sources.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · CG Bio Co., Ltd. · Hwaseong · plastic-surgery device · refused as adulteration, misbranding
- MONITORWIMulti-topicAug 10, 2026
WI State Administrative Register: Emergency Rules Filed with Legislative Reference Bureau - 2026-08-10
Emergency rules may impact licensure practices in Wisconsin.
What to do — members only.Become a member →State Administrative Registerprimary source ↗ - MONITORFEDAesthetic InjectablesFDA: VAIAug 10, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refused entry of OnabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Hugel Inc. · Chuncheon · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 10, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses collagen implant shipment from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Across Co., Ltd · Chuncheon-si · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIAug 10, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry of Onabotulinumtoxina from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daewoong Pharmaceutical Co. Ltd. (Hyangnam factory) · Hwaseong · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesAug 7, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refuses entry for collagen implants from Sweden.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesAug 7, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA rejects dermal collagen implants from South Korea; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Inc. · Cheongju · plastic-surgery device · refused entry by FDA
- CAUTIONILMulti-topicAug 7, 2026
IL HB5000: Health Facilities Planning
Ownership rules for health care facilities in Illinois affect med spas.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDAesthetic InjectablesFDA: VAIAug 7, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Ireland)
FDA refused OnabotulinumtoxinA shipment.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Pharmaceuticals Ireland · Westport · drug product · refused entry by FDA · FDA lab-analyzed
- MONITORFEDAesthetic InjectablesAug 6, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA denies entry of foreign collagen implants for aesthetics.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Across Co., Ltd · Chuncheon-si · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIAug 4, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Ireland)
OnabotulinumtoxinA from Ireland refused entry to the US.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Pharmaceuticals Ireland · Westport · drug product · refused as unapproved new drug · FDA lab-analyzed
- MONITORFEDAesthetic InjectablesAug 4, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
Collagen implants from France denied entry to the US by FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · LABORTORIES FILLMED · Paris-L'Hopital · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesAug 3, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of dermal collagen imports from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · SEORIN COMPANY CO LTD · Chuncheon · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesAug 3, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refused shipment of OnabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Inc. · Cheongju · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIAug 3, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Ireland)
FDA refuses entry of injectable product ONABOTULINUMTOXINA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Pharmaceuticals Ireland · Westport · drug product · refused entry by FDA · FDA lab-analyzed
- MONITORFEDAesthetic InjectablesAug 3, 2026
FDA import refusal: Solution, Sodium Hyaluronate (South Korea)
FDA refuses entry for sodium hyaluronate from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Dongkook Pharmaceutical Co., Ltd. · Seoul · medical device · refused as misbranding, adulteration
- MONITORWIMulti-topicAug 3, 2026
WI State Administrative Register: 848A1 Register (8/3/2026) - 2026-08-03
Wisconsin nursing rule update may impact med spa regulations.
What to do — members only.Become a member →State Administrative Registerprimary source ↗ - MONITORFEDAesthetic InjectablesFDA: VAIJul 31, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Ireland)
FDA refuses entry of onabotulinumtoxinA from Ireland.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Pharmaceuticals Ireland · Westport · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIJul 31, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses OnabotulinumtoxinA shipment from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daewoong Pharmaceutical Co. Ltd. (Hyangnam factory) · Hwaseong · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 31, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry for collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · WEDERM · Seoul · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesJul 31, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refuses entry of dermal collagen implants from Sweden.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused entry by FDA
- MONITORFEDGLP-1 CompoundingJul 31, 2026
FDA import refusal: Tirzepatide (Anti-diabetic) (Vietnam)
FDA refuses entry of Tirzepatide from Vietnam; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · NGUYEN VIET ANH - CCCD#035094002294 · Hanoi Center · drug product · refused as unapproved new drug
- MONITORFEDMulti-topicJul 31, 2026
Primary Source Monitoring: Illinois Man and Indiana Woman Sentenced Respectively to 70 Months and 16 Months in Prison For Selling Unapproved Drugs in Interstate Commerce
Sentencing for selling unapproved drugs serves as a warning.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesJul 31, 2026
FDA import refusal: Lidocaine (Guatemala)
Lidocaine from Guatemala refused entry by FDA; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · SELECTPHAMA · Mixco · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIJul 31, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use
FDA refuses entry of collagen implants for aesthetic use.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Revance Therapeutics, Inc · Newark · plastic-surgery device · refused as misbranding
- MONITORFEDGLP-1 CompoundingJul 30, 2026
FDA / Federal Register Notice: Outsourcing Facility Fee Rates for Fiscal Year 2027
FDA fees for outsourcing facilities will impact med spas using compounds.
What to do — members only.Become a member →Federal Registerprimary source ↗ - MONITORFEDAesthetic InjectablesJul 29, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Pharmaresearch · Gangneung-si · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 27, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refused entry for a collagen implant from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ACROSS CO LTD · Chuncheon-Si · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 27, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry of ONABOTULINUMTOXINA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Meditox Co. · Heungdeok-gu · drug product · refused as misbranding
- MONITORFEDGLP-1 CompoundingJul 27, 2026
FDA import refusal: Tirzepatide (Anti-diabetic) (Japan)
FDA blocks tirzepatide shipment from Japan.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Eli Lilly Japan K.K.Seishin Laboratories · Nishigun · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIJul 27, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry of injectable product from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daewoong Pharmaceutical Co. Ltd. (Hyangnam factory) · Hwaseong · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesJul 27, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry of ONABOTULINUMTOXINA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · PharmaResearch BIO Co., Ltd. · Gangreung · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: VAIJul 27, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses import of OnabotulinumtoxinA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Hugel Inc. · Chuncheon · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesJul 27, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of dermal collagen implant from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · BioPlus Co.,Ltd. · Seongnam · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 27, 2026
FDA import refusal: Lidocaine (South Korea)
FDA refuses entry of lidocaine from South Korea; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Vivozon Pharmaceutical · Hwaseong · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesJul 25, 2026
FDA import refusal: Acid, Hyaluronic, Intraarticular (Sweden)
FDA refuses entry of hyaluronic acid from Sweden for unknown violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-MED AB · Sweden · medical device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Switzerland)
FDA refuses entry of collagen dermal implants from Switzerland.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Teoxane S.A. · Geneva · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses entry of French collagen implant for aesthetics.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ALLERGAN · Annecy · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of aesthetic collagen implant from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · HNG Co., Ltd. · Seocho · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Vietnam)
FDA refuses entry of OnabotulinumtoxinA from Vietnam; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · TRAN THI THU HIEN · Ha Noi City · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refused entry of collagen implants from Sweden; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Switzerland)
FDA refuses entry of dermal collagen implant from Switzerland.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ANTEIS SA · Plan-les-Ouates · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA blocks import of dermal collagen from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Forest Hills Lab Korea Co Ltd · Gyeonggi-do · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses shipment of aesthetic collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · SEORIN COMPANY CO LTD · Chuncheon · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA rejects botulinum toxin import from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · PharmaResearch BIO Co., Ltd. · Gangreung · drug product · refused entry by FDA
- MONITORFEDGLP-1 CompoundingFDA: VAIJul 24, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (Denmark)
FDA refused entry of semaglutide from Denmark.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Novo Nordisk A/S · Bagsvard · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Austria)
FDA refuses entry of collagen implants from Austria; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · CROMA-PHARMA GMBH · Leobendorf · plastic-surgery device · refused entry by FDA
- MONITORFEDGLP-1 CompoundingJul 24, 2026
FDA import refusal: Tirzepatide (Anti-diabetic) (China)
FDA rejects tirzepatide shipment from China due to violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · CHONGUHAN MEDICAL TECHNOLOGIES · Guangzhou · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry for dermal collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Pharmaresearch · Gangneung-si · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA blocks botulinum toxin from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Meditox Co. Ltd. · Unknown · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIJul 24, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Germany)
FDA refuses entry for OnabotulinumtoxinA from Germany.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Merz Pharma Gmbh & Co. KGaA · Reinheim · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses shipment of collagen implant from France.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Industrie SAS · Pringy · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Lidocaine (China)
FDA refuses lidocaine shipment from China due to violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Shaanxi Bieyouth Biotech Co.,Ltd · Xian · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesJul 24, 2026
FDA import refusal: Triamcinolone Acetonide (Glucocorticoid) (Guatemala)
FDA refuses Guatemala-sourced triamcinolone acetonide shipment.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · LABORATORIO PIERSAN S.A. · Cdad · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIJul 24, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (United Kingdom)
FDA refuses ONABOTULINUMTOXINA import; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Ipsen BioPharm Ltd · Wrexham · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: VAIJul 24, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use
Collagen implant shipment refused by FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Merz North America, Inc. · Franksville · plastic-surgery device · refused as misbranding
- MONITORFEDGLP-1 CompoundingJul 22, 2026
FDA import refusal: Tirzepatide (Anti-diabetic) (India)
FDA rejects tirzepatide import from India.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ELI LILLY AND COMPANY PVT LTD · Bhiwandi · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesJul 22, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Vietnam)
FDA refuses entry of dermal collagen implant from Vietnam.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · TRAN THI THU HIEN · Ha Noi City · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDGLP-1 CompoundingFDA: VAIJul 21, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (Denmark)
FDA rejects semaglutide shipment from Denmark; verify supplier sources.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Novo Nordisk A/S · Bagsvard · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesFDA: OAIJul 21, 2026
FDA import refusal: Lidocaine (Belgium)
FDA refuses entry of lidocaine from Belgium.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Laboratoria Qualiphar NV · Bornem · drug product · refused as adulteration
- MONITORFEDAesthetic InjectablesJul 21, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Vietnam)
FDA rejects injectable collagen from Vietnam due to violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · CHIAKI TRADING JSC · Hanoi City · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDMulti-topicJul 17, 2026
Primary Source Monitoring: Wilson v. Lexington Compounding Pharmacy, Inc. (5:26-cv-00273) — District Court, E.D. Kentucky
No immediate changes for med spas from recent court case findings.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesJul 17, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Colombia)
FDA refuses entry of Colombian dermal collagen implant.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · GALDERMA DE COLOMBIA SA · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesFDA: VAIJul 16, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Ireland)
FDA refuses entry of OnabotulinumtoxinA from Ireland.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Pharmaceuticals Ireland · Westport · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 16, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refuses entry of Swedish collagen implant for aesthetics.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 14, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
Important: FDA refuses dermal implant shipment from Sweden.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · MARELI MEDICAL AB · Malmo · plastic-surgery device · refused entry by FDA
- MONITORFEDGLP-1 CompoundingJul 13, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (United Kingdom)
FDA refuses entry of injectable Semaglutide from the UK.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ASIAN SUITS ONLINE LIMITED · Leicester · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesJul 11, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses entry of collagen implants from France.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ALLERGAN · Annecy · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 11, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry for collagen dermal implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · SEORIN COMPANY CO LTD · Chuncheon · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: VAIJul 10, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses entry of collagen implant from France; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Industrie SAS · Pringy · plastic-surgery device · refused as misbranding
- MONITORFEDGLP-1 CompoundingJul 10, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (Canada)
FDA refuses semaglutide shipment from Canada; avoid gray-market sources.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · NOVO NORDISK · Mississauga · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesJul 10, 2026
FDA import refusal: Botox (onabotulinumtoxinA)
FDA refuses entry of OnabotulinumtoxinA from Illinois due to violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · AbbVie Inc. · North Chicago · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesJul 10, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refuses entry of a dermal collagen implant from Sweden.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesJul 10, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Germany)
Injectable collagen implants from Germany denied entry by FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Merz Pharmaceuticals GmbH · Frankfurt Am Main · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIJul 10, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses ONABOTULINUMTOXINA from South Korea; verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Daewoong Pharmaceutical Co. Ltd. (Hyangnam factory) · Hwaseong · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesJul 10, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Italy)
FDA refuses entry for collagen implants from Italy; check your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · IBSA Farmaceutici Italia Srl · Lodi · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 10, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (India)
FDA rejects ONABOTULINUMTOXINA from India.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · HIMANI BIOSCIENCES · Solan · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesJul 10, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Italy)
FDA refuses entry of Italian collagen implants.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Mariior · Marignano · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 9, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of South Korean collagen dermal implants.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · BNC Global · Incheon · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIJul 8, 2026
FDA import refusal: Daxxify (daxibotulinumtoxinA)-LANM
FDA refuses entry for DAXIBOTULINUMTOXINA-LANM; avoid unverified sources.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Revance Therapeutics, Inc · Newark · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 8, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refuses entry of collagen implants from Sweden; heed sourcing warnings.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused entry by FDA
- CRITICALFEDMulti-topicFDA: OAIJul 8, 2026
FDA Warning Letter: Spa De Soleil, Inc. (Drugs)
Water Spa De Soleil uses to make over-the-counter topical products failed testing 51 times from 2024 to 2025. FDA had cited similar problems in 2021.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - MONITORFEDAesthetic InjectablesJul 8, 2026
FDA import refusal: Implant, Dermal, for Aesthetic Use in the Hands (Sweden)
FDA refuses dermal implant entry from Sweden.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Q-Med AB · Uppsala · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 8, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Brazil)
FDA refuses Brazilian collagen implant shipment.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Pharmaesthetics do Brasil Industria de Medicamentos LTDA · Zielonka · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 8, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses entry of overseas collagen implant.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Sinclair France SAS · Dardilly · plastic-surgery device · refused entry by FDA
- MONITORFEDGLP-1 CompoundingJul 7, 2026
FDA import refusal: Tirzepatide (Anti-diabetic) (United Kingdom)
FDA refuses entry of TIRZEPATIDE from the UK; verify suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ARAMEX- TRANSIT · Slough · drug product · refused as adulteration
- MONITORFEDAesthetic InjectablesJul 7, 2026
FDA import refusal: Solution, Sodium Hyaluronate (Paraguay)
Product shipment from Paraguay refused by FDA; heed sourcing warnings.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · FABIANO DA SILVA MATOS · Ciudad Del Este · medical device · refused as misbranding
- MONITORFEDAesthetic InjectablesJul 6, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses entry for collagen implants from France.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan · Pringy 74370 Annecy · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 6, 2026
FDA import refusal: Lidocaine (Sweden)
FDA refuses entry of lidocaine shipment from Sweden.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · MARELI MEDICAL AB · Malmo · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: VAIJul 6, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use
FDA refused entry of dermal collagen implants on July 6, 2026.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Merz North America, Inc. · Franksville · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 5, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of injectable collagen from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · SEORIN COMPANY CO LTD · Chuncheon · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: VAIJul 2, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (United Kingdom)
FDA bars entry of ONABOTULINUMTOXINA from the UK.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Ipsen BioPharm Ltd · Wrexham · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesJul 2, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Vietnam)
FDA refuses ONABOTULINUMTOXINA shipment from Vietnam.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · TRAN THI THU HIEN · Ha Noi City · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 2, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Vietnam)
FDA refuses shipment of collagen implant from Vietnam.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · CHIAKI TRADING JSC · Hanoi City · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 2, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Switzerland)
Imported collagen implants from Switzerland were refused by the FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · GALDERMA LABORATORIES · Lausanne · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 2, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA rejects collagen implants from South Korea; check your sources.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · LG Chemical LTD. · Seoul · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 2, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA denies entry to a dermal collagen implant from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · BioPlus Co.,Ltd. · Seongnam · plastic-surgery device · refused as misbranding, adulteration
- MONITORFEDAesthetic InjectablesJul 2, 2026
FDA import refusal: Lidocaine (India)
FDA refuses entry of lidocaine from India.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ARISTO PHARMACEUTICALS · Mumbai · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesJul 2, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses ONABOTULINUMTOXINA from South Korea; review your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Inc. · Cheongju · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesJul 2, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses OnabotulinumtoxinA shipment from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Medytox Inc. · Cheongju · drug product · refused as misbranding, unapproved new drug
- MONITORFEDMulti-topicJul 1, 2026
Primary Source Monitoring: Massachusetts Couple Sentenced to Prison for Importing Misbranded Drugs From China and Selling Them to Customers in U.S. for Performance Enhancing Pu…
A couple was sentenced for selling misbranded drugs in the U.S.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesFDA: VAIJun 30, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (United Kingdom)
FDA refuses ONABOTULINUMTOXINA from overseas; verify your supplier.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Ipsen BioPharm Ltd · Wrexham · drug product · refused entry by FDA
- MONITORFEDGLP-1 CompoundingJun 30, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (China)
FDA refuses entry of semaglutide from China.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Hybio Pharmaceutical Co., Ltd. · Shenzhen · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesJun 30, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Vietnam)
FDA refuses entry of OnabotulinumtoxinA from Vietnam.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · HASAKI BEAUTY & CLINIC JSC · Hanoi City · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesJun 30, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Sweden)
FDA refuses entry of collagen implant from Sweden—stay cautious.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · MARELI MEDICAL AB · Malmo · plastic-surgery device · refused entry by FDA
- MONITORFEDAesthetic InjectablesFDA: VAIJun 29, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (France)
FDA refuses entry of French collagen implant due to violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Industrie SAS · Pringy · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: OAIJun 29, 2026
FDA import refusal: Lidocaine Hcl (Anesthetic) (India)
FDA refuses entry of Lidocaine HCl from India; stay cautious.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Mahendra Chemicals · Ahmedabad · drug product · refused as adulteration
- MONITORFEDAesthetic InjectablesJun 29, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Turkey)
FDA refuses entry of OnabotulinumtoxinA from Turkey.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · ALLERGAN ILACLARI TICARET A.S. · Sariyer · drug product · refused as misbranding, unapproved new drug
- MONITORFEDMulti-topicJun 29, 2026
Primary Source Monitoring: Pagan v. Glow Med Spa (1:26-cv-24474) — District Court, S.D. Florida
Americans with Disabilities Act lawsuit filed against a Florida med spa.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesFDA: VAIJun 29, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Ireland)
FDA refuses ONABOTULINUMTOXINA entry from Ireland — verify your suppliers.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Allergan Pharmaceuticals Ireland · Westport · drug product · refused entry by FDA
- MONITORFEDAesthetic InjectablesJun 29, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (Germany)
FDA refuses entry of German botulinum toxin.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Merz Pharmaceuticals GmbH · Frankfurt Am Main · drug product · refused entry by FDA
- MONITORFEDGLP-1 CompoundingJun 29, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (India)
FDA refuses entry of semaglutide from India.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · NOVO NORDISK INDIA PRIVATE LIMIT · Bangalore · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesJun 29, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
Shipment of collagen implants from South Korea refused by FDA.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Jemate · Gyeonggi-do · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesJun 29, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (Vietnam)
FDA blocks vital aesthetic product from Vietnam due to violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · CHIAKI TRADING JSC · Hanoi City · plastic-surgery device · refused as adulteration
- MONITORFEDAesthetic InjectablesJun 29, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA blocks import of a dermal collagen implant from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · LG Chem., Ltd. · Iksan · plastic-surgery device · refused as misbranding
- MONITORFEDAesthetic InjectablesFDA: VAIJun 26, 2026
FDA import refusal: Lidocaine (China)
FDA refuses lidocaine shipment from China due to violations.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Planet (Anhui) Pharmaceuticals Co., Ltd · Chuzhou · drug product · refused as misbranding
- MONITORFEDAesthetic InjectablesJun 26, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of collagen implants from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · BNC INTERNATIONAL · Incheon · plastic-surgery device · refused entry by FDA
- MONITORFEDGLP-1 CompoundingJun 26, 2026
FDA import refusal: Semaglutide (Anti-diabetic) (India)
FDA refuses entry of Semaglutide from India.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · AULI KRUPA · Mumbai · drug product · refused as unapproved new drug
- MONITORFEDAesthetic InjectablesJun 26, 2026
FDA import refusal: Implant, Dermal, Collagen for Aesthetic Use (South Korea)
FDA refuses entry of foreign dermal implant; stay vigilant.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · HUGEL CO LTD · Gangnam · plastic-surgery device · refused entry by FDA
- MONITORFEDGLP-1 CompoundingJun 26, 2026
FDA / Federal Register Notice: List of Bulk Drug Substances for Which There Is a Clinical Need Under Section 503B of the Federal Food, Drug, and Cosmetic Act; Extension of Comment Period
FDA extends comment period on GLP-1 compounding decisions.
What to do — members only.Become a member →Federal Registerprimary source ↗ - CAUTIONALMulti-topicJun 25, 2026
AL Primary Source Monitoring: Proposed Rule Changes
Stay informed about proposed rule changes in Alabama.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDAesthetic InjectablesJun 24, 2026
FDA import refusal: Triamcinolone (Glucocorticoid) (Guatemala)
FDA rejects triamcinolone shipment from Guatemala.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Infasa · Mixco · drug product · refused as misbranding, unapproved new drug
- MONITORFEDAesthetic InjectablesJun 24, 2026
FDA import refusal: Lidocaine Hcl (Anesthetic) (South Korea)
FDA refuses shipment of Lidocaine HCL from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Huons Co., Ltd. · Jecheon · drug product · refused as adulteration
- MONITORFEDAesthetic InjectablesFDA: VAIJun 23, 2026
FDA import refusal: Botox (onabotulinumtoxinA) (South Korea)
FDA refuses entry of ONABOTULINUMTOXINA from South Korea.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Hugel Inc. · Chuncheon · drug product · refused entry by FDA
- CAUTIONFEDMulti-topicJun 23, 2026
FDA Warning Letter: ketaminelab.org (Drugs)
FDA says buyketaminepowderonline.com (formerly ketaminelab.org) sells unapproved, misbranded ketamine powder online.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - MONITORFEDGLP-1 CompoundingJun 23, 2026
FDA import refusal: Tirzepatide (Anti-diabetic) (Bangladesh)
FDA refuses TIRZEPATIDE import from Bangladesh; details pending.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Drug Internatinal Gazipur Bangladesh · Dhaka · drug product · refused as misbranding
- MONITORFEDGLP-1 CompoundingFDA: OAIJun 22, 2026
FDA import refusal: Semaglutide (Anti-diabetic)
FDA refused entry of a semaglutide shipment due to violation.
What to do — members only.Become a member →FDA Import RefusalFDA Import Refusals database ↗FDA record · Novo Nordisk Inc. · Plainsboro · drug product · refused as unapproved new drug
- CAUTIONFEDPeptidesJun 17, 2026
FDA Warning Letter: Wholesale Peptide (Drugs)
FDA says Wholesale Peptide's injectable "Prostamax" and gonadorelin are unapproved new drugs.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - CAUTIONFEDGLP-1 CompoundingJun 17, 2026
FDA Warning Letter: Herbal Dermals Ltd (Drugs)
Herbal Dermals Ltd received an FDA Warning Letter; verify details.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - CAUTIONFEDMulti-topicJun 17, 2026
FDA Warning Letter: Herbal Dermals LLC Fz (Drugs)
FDA says Gotucream, sold online as a balanitis treatment cream, is an unapproved new drug.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - CAUTIONFEDGLP-1 CompoundingJun 17, 2026
FDA Warning Letter: Herbal Dermals Ltd (Drugs)
FDA issued a Warning Letter to Herbal Dermals Ltd.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - CAUTIONFEDGLP-1 CompoundingJun 17, 2026
FDA Warning Letter: Herbal Dermals Ltd (Drugs)
FDA Warning Letter issued to Herbal Dermals Ltd.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - CAUTIONFEDMarketing & AdvertisingJun 12, 2026
FTC Files Contempt Motion Against Amare Global and Three Individuals Over Unsubstantiated Health Claims
FTC targets deceptive health claims affecting aesthetic practices.
What to do — members only.Become a member →FTC Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingJun 11, 2026
FDA shortage: Liraglutide Injection (Injection) — Currently in Shortage
Liraglutide remains compounded under shortage status.
What to do — members only.Become a member →FDA Drug Shortagesprimary source ↗ - MONITOROHScope of PracticeJun 9, 2026
OH HB963: Revise the law governing the practice of physician assistants
Changes to PAs' practice could affect med spa operations.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORGAMulti-topicJun 5, 2026
GA State Medical Board: Gcmb Statement Regarding: IV Hydration/Therapy Position Statement | June 5, 2026
Georgia issues a position statement on IV hydration therapy.
What to do — members only.Become a member →State Medical Boardprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIJun 5, 2026
FDA inspection citations: Pillar5 Pharma Inc. (4 observations)
FDA cites Pillar5 Pharma for sterile production issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - CRITICALFEDGLP-1 CompoundingMay 27, 2026
FDA recall (Class II): Liraglutide Injection, 18 mg/3 mL (6 mg/mL), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, Fl 34108, …
FDA recalls contaminated Liraglutide Injection.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORCAGLP-1 CompoundingMay 27, 2026
CA SB1089: Preventive Treatment Health Care Act.
California bill to have the state negotiate GLP-1 anti-obesity drug pricing; sent to the Governor.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingMay 26, 2026
FDA / Federal Register Notice: Agency Information Collection Activities; Proposed Collection; Comment Request; Human Drug Compounding Under Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act
FDA seeks comments on human drug compounding regulations.
What to do — members only.Become a member →Federal Registerprimary source ↗ - MONITORMAScope of PracticeMay 26, 2026
MA H5455: Regulating the operation of medical spas
Proposed Massachusetts bill to regulate the operation of med spas.
What to do — members only.Become a member →LegiScanprimary source ↗ - CAUTIONFEDGLP-1 CompoundingMay 26, 2026
Primary Source Monitoring: Agency Information Collection Activities; Proposed Collection; Comment Request; Human Drug Compounding Under Sections 503A and 503B of the Federal Fo…
FDA requests comments on drug compounding information collection.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIMay 21, 2026
FDA inspection citations: Oakwood Laboratories LLC (4 observations)
FDA cites Oakwood Laboratories for quality and sterility issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORGAMulti-topicMay 19, 2026
GA State Medical Board: IV Hydration/Therapy Position Statement
Georgia board issues guidance on IV hydration therapies.
What to do — members only.Become a member →State Medical Boardprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIMay 19, 2026
FDA inspection citations: Novartis Pharma Stein AG (2 observations)
FDA cites Novartis Pharma for sterility issues; verify sourcing.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDNeuromodulatorsMay 19, 2026
Primary Source Monitoring: California Doctor Convicted of $45M Botox Fraud Scheme Targeting Medicare
California doctor convicted in Botox fraud scheme.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIMay 19, 2026
FDA inspection citations: Samchundang Pharm Co., Ltd. (8 observations)
FDA cites facility for sterile compounding issues; verify your sources.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIMay 15, 2026
FDA inspection citations: Unither Manufacturing LLC. (9 observations)
FDA cites Unither Manufacturing for issues related to sterility.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIMay 15, 2026
FDA inspection citations: Emcure Pharmaceuticals Limited (7 observations)
FDA cites Emcure Pharmaceuticals for sterile process issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIMay 15, 2026
FDA inspection citations: Owen Biosciences Inc. (3 observations)
FDA cites Owen Biosciences for quality control violations.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIMay 13, 2026
FDA inspection citations: InvaTech Pharma Solutions, LLC (6 observations)
Med spas should verify sourcing from InvaTech Pharma Solutions.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - CRITICALFEDGLP-1 CompoundingFDA: OAIMay 12, 2026
FDA Warning Letter: Fresenius Kabi Compounding, LLC (Drugs)
FDA Warning Letter issued to Fresenius Kabi Compounding, LLC.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - MONITORFEDMulti-topicMay 8, 2026
Primary Source Monitoring: Med Spa Owner Pleads Guilty to Performing Illegal Injections Using Unapproved Prescription Drugs
Guilty plea highlights risks of using unapproved injections.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIMay 5, 2026
FDA inspection citations: Zydus Lifesciences Limited (7 observations)
FDA cites Zydus Lifesciences for sterility and quality issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIMay 4, 2026
FDA inspection citations: Element Materials Technology Boston - Acton Inc. (4 observations)
Caution urged for med spas sourcing from a cited facility.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIMay 1, 2026
FDA inspection citations: SnugZ USA, Inc. (9 observations)
FDA cites SnugZ USA for quality control issues; verify your supply.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIMay 1, 2026
FDA inspection citations: Gvs Tm, Inc (14 observations)
FDA cites GVS TM, Inc; verify sourcing and remediation.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingMay 1, 2026
FDA / Federal Register Notice: List of Bulk Drug Substances for Which There Is a Clinical Need Under Section 503B of the Federal Food, Drug, and Cosmetic Act
FDA evaluates bulk drug substances; GLP-1 agents may be impacted.
What to do — members only.Become a member →Federal Registerprimary source ↗ - MONITORFEDGLP-1 CompoundingApr 30, 2026
FDA / Federal Register Notice: Determination That Ozempic (Semaglutide) Solution, 2 Milligrams Per 1.5 Milliliters Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness
FDA ensures continued access to OZEMPIC for aesthetic practices.
What to do — members only.Become a member →Federal Registerprimary source ↗ - MONITORFEDMulti-topicApr 30, 2026
Primary Source Monitoring: Advisory Committee; Pharmacy Compounding Advisory Committee; Renewal
Pharmacy Compounding Advisory Committee renewed for continued oversight.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIApr 29, 2026
FDA inspection citations: American Red Cross Manchester Fixed Site (1 observation)
FDA cites facility for sterility issues impacting med spas.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIApr 29, 2026
FDA inspection citations: Samson Pharmaceuticals, Inc (8 observations)
FDA cites Samson Pharmaceuticals for multiple compliance issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIApr 24, 2026
FDA inspection citations: Hanlim Pharm Co. Ltd. (11 observations)
FDA cites Hanlim Pharm for sterility and validation issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIApr 24, 2026
FDA inspection citations: University of Vermont Health Network - Adirondack Blood Center (2 observations)
FDA cites facility for sterility issues; verify your sources.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORCOMulti-topicApr 23, 2026
CO SB130: Medical Spas Deceptive Trade Practices
Colorado med spa drug-practices bill; postponed indefinitely in committee.
What to do — members only.Become a member →LegiScanprimary source ↗ - CRITICALTNNATIONALScope of PracticeApr 23, 2026
TN HB2044: an Act to amend Tennessee Code Annotated, Title 63; Title 68, Chapter 11, Part 2 and Chapter 1042 of the Public Acts of 2024, relative to certified medical assistants.
Tennessee HB 2044 on delegating aesthetic injections to certified MAs.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORTNScope of PracticeApr 23, 2026
TN SB2548: an Act to amend Tennessee Code Annotated, Title 63; Title 68, Chapter 11, Part 2 and Chapter 1042 of the Public Acts of 2024, relative to certified medical assistants.
Med spas can delegate botulinum toxin tasks to certified medical assistants.
What to do — members only.Become a member →LegiScanprimary source ↗ - CRITICALFEDMulti-topicFDA: OAIApr 22, 2026
FDA Warning Letter: Active Cosmetics Manufacturing Inc (Drugs)
FDA cites Active Cosmetics Manufacturing for releasing OTC topical drugs after failed microbial tests, including S. aureus.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - MONITORFEDGLP-1 CompoundingApr 22, 2026
FDA recall (Class II): Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML, 0.5 mL vials, Rx only, Northwest Compounders, Bea…
FDA recalls semaglutide compound over sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIApr 21, 2026
FDA inspection citations: Altaire Pharmaceuticals, Inc. (8 observations)
Caution: FDA cites facility for sterility issues; verify your sources.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - CAUTIONFEDMulti-topicFDA: OAIApr 20, 2026
FDA Warning Letter: Foshan Miwei Cosmetics Co., Ltd. (Drugs)
FDA cites Foshan Miwei Cosmetics for releasing OTC drug products without testing active-ingredient strength or microbes.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - MONITORFEDGLP-1 CompoundingApr 16, 2026
Primary Source Monitoring: Pharmacy Compounding Advisory Committee; Notice of Meeting; Establishment of a Public Docket; Request for Comments-Bulk Drug Substances Nominated for…
Pharmacy Compounding Advisory Committee discusses new bulk substances.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIApr 14, 2026
FDA inspection citations: Rohto-Mentholatum (Vietnam) Co., Ltd. (8 observations)
FDA cites sterile compounder for product quality concerns.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORCTScope of PracticeApr 9, 2026
CT HB05399: An Act Concerning Dentistry.
CT bill updates dental assistant regulations for aesthetic procedures.
What to do — members only.Become a member →LegiScanprimary source ↗ - CAUTIONMEMulti-topicApr 8, 2026
ME LD2201: An Act to Implement Certain Recommendations Related to the Regulatory Review and Approval of Certain Health Care Transactions Involving Private Equity Companies, Hedge Funds or Management Services Organizations from the Commission to Evaluate the Scope of Regulatory Review and Oversight over Health Care Transactions That Impact the Delivery of Health Care Services in the State
Notification rules impact med spas working with private equity.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDMulti-topicApr 7, 2026
Primary Source Monitoring: Med Spa Owner Pleads Guilty to Performing Thousands of Injections Using Counterfeit Products
Med spa owner guilty of using counterfeit injection products.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIApr 2, 2026
FDA inspection citations: Baxter Healthcare Corporation (9 observations)
FDA cites Baxter for sterility concerns; verify your sources.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - CAUTIONFEDMulti-topicApr 2, 2026
FDA Warning Letter: Purolea Cosmetics Lab (Drugs)
FDA cites Purolea Cosmetics Lab for insects and filth in its plant and for untested homeopathic drug products.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - MONITORFEDScope of PracticeApr 1, 2026
Primary Source Monitoring: Utah Licensed Osteopathic Physician Indicted for Allegedly Receiving Misbranded Drugs from China and Selling them to Patients
Indictment of a physician raises concerns for med spas on drug sourcing.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - CAUTIONFEDMulti-topicApr 1, 2026
FDA Warning Letter: Pure Indulgence Aesthetics (Drugs)
FDA says a Texas med spa administered far more Botox than it bought from AbbVie, and so had sourced toxin from unauthorized suppliers.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - CAUTIONFEDGLP-1 CompoundingMar 31, 2026
FDA Warning Letter: Mile High Compounds (Drugs)
FDA says the "research-only" semaglutide, tirzepatide and retatrutide sold by Mile High Compounds are unapproved injectable drugs. The firm's own weight-loss dosing guides, shared through its online forum, were FDA's evidence that the products were meant for people.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - CAUTIONFEDGLP-1 CompoundingMar 31, 2026
FDA Warning Letter: Gram Peptides (Drugs)
FDA says GRAM Peptides' "research use only" retatrutide and tirzepatide, sold with bacteriostatic water, are unapproved drugs.
What to do — members only.Become a member →FDA Warning Letterprimary source ↗ - MONITORKYScope of PracticeMar 27, 2026
KY HB885: an Act relating to cosmetology.
Supervision requirements for esthetic practices in Kentucky.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIMar 19, 2026
FDA inspection citations: PReye LLC (4 observations)
Med spas should check sourcing from PReye LLC after FDA findings.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - CAUTIONFEDAesthetic DevicesMar 18, 2026
FDA device recall (Class II): Clarity II Laser System; Model No. 1110200210.
FDA recalls Clarity II Laser System for safety concerns.
What to do — members only.Become a member →FDA Device Recallprimary source ↗ - MONITORFLMulti-topicMar 13, 2026
FL S1728: Licensure of Medical Spas
Proposed licensure for medical spas would enhance oversight and compliance.
What to do — members only.Become a member →LegiScanprimary source ↗ - CAUTIONFLScope of PracticeMar 13, 2026
FL H1429: Licensure of Medical Spas
Florida med spa licensure bill; died in subcommittee.
What to do — members only.Become a member →LegiScanprimary source ↗ - CAUTIONFEDGLP-1 CompoundingMar 11, 2026
FDA recall (Class II): Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 843…
FDA recalls specific compounded GLP-1 products due to quality issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingMar 11, 2026
FDA recall (Class II): Tirzepatide Inj, 10mg, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, Ks 66061, NDC …
FDA recalls Tirzepatide injection over sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingMar 11, 2026
FDA recall (Class II): Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 843…
Important recall on compounded Semaglutide products affecting med spas.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - CRITICALFEDGLP-1 CompoundingMar 11, 2026
FDA recall (Class II): Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, Ks 66061,…
FDA recalls Semaglutide for sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingMar 11, 2026
FDA recall (Class II): Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, Ks 66061, …
FDA recalls compounded GLP-1 product over sterility concerns.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - CAUTIONFEDGLP-1 CompoundingMar 11, 2026
FDA recall (Class II): Tirzepatide Inj, 15mg x 4, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, Ks 66061, …
FDA recalls Tirzepatide Inj over sterility concerns.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIMar 6, 2026
FDA inspection citations: Pharmaceutics International, Inc. (9 observations)
FDA cites compounding facility for sterility and quality concerns.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - CAUTIONINNATIONALMulti-topicMar 5, 2026
IN SB0282: Compounding drugs; registration of medical spas.
Indiana med spas must register with the licensing board by Jan 1, 2027.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIMar 5, 2026
FDA inspection citations: Sharp Sterile Manufacturing, LLC (6 observations)
FDA cites facility for sterilization and procedural issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORWVScope of PracticeMar 2, 2026
WV SB486: Relating to Wv Board of Barbers and Cosmetologists
'Master aesthetician' role expands service capabilities in WV.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIFeb 27, 2026
FDA inspection citations: Gallant Pet Inc (10 observations)
FDA inspection reveals sterility issues at Gallant Pet Inc.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIFeb 27, 2026
FDA inspection citations: Tan-Alize Kozmetik ve Temizlik Urunleri Sanayi ve Ticaret A.S. (7 observations)
FDA inspection reveals quality concerns for a facility supplying med spas.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIFeb 27, 2026
FDA inspection citations: Gasco Industrial Corp. (13 observations)
FDA cites facility for issues potentially affecting product quality.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIFeb 26, 2026
FDA inspection citations: CoreRX Inc. (7 observations)
FDA cites CoreRX Inc. for multiple quality control issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFeb 23, 2026
FDA / Federal Register Notice: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Human Drug Compounding Under Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act
FDA notice may impact GLP-1 compounding practices at med spas.
What to do — members only.Become a member →Federal Registerprimary source ↗ - MONITORFEDGLP-1 CompoundingFeb 23, 2026
Primary Source Monitoring: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Human Drug Compounding Under Sectio…
Comment period open on federal compounding information requirements.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIFeb 20, 2026
FDA inspection citations: Staska Pharmaceuticals, Inc. (3 observations)
FDA cites Staska Pharmaceuticals for quality and sterility issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIFeb 18, 2026
FDA inspection citations: Gilead Sciences, Inc. (7 observations)
FDA cites Gilead Sciences for sterility and quality control issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORWVScope of PracticeFeb 16, 2026
WV HB5538: To expand licensing opportunities and safety regulation in the esthetics industry
Licensing bill expands esthetics practices in WV.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIFeb 13, 2026
FDA inspection citations: K.C. Pharmaceuticals, Inc (13 observations)
FDA cites K.C. Pharmaceuticals for sterility concerns.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORRIOwnership/CPOMFeb 12, 2026
RI H7721: Establishes the Rhode Island Ban on the Corporate Practice of Medicine Act.
RI Bill H7721 may change corporate practice for med spas.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIFeb 12, 2026
FDA inspection citations: Tropical Seas, Inc. (8 observations)
FDA cites Tropical Seas for multiple quality concerns.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORAZScope of PracticeFeb 10, 2026
AZ HB4047: Medical spas; licensure; regulation
Licensure requirements for med spas in Arizona.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIFeb 6, 2026
FDA inspection citations: Csl Plasma Inc (2 observations)
FDA cites CSL Plasma for contamination and product deviation issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIFeb 6, 2026
FDA inspection citations: Eugia Pharma Specialities Limited (11 observations)
FDA cites Eugia Pharma for serious sterility issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIFeb 6, 2026
FDA inspection citations: Alcami Carolinas Corporation (6 observations)
Check sourcing from Alcami Carolinas after FDA citations.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORRIOwnership/CPOMFeb 6, 2026
RI S2459: Establishes the Rhode Island Ban on the Corporate Practice of Medicine Act.
Rhode Island's S2459 could impact med spa ownership practices.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIFeb 5, 2026
FDA inspection citations: Nice-Pak Products, LLC (4 observations)
FDA cites Nice-Pak Products for facility inspection issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORILOwnership/CPOMFeb 5, 2026
IL SB3463: Health Facilities Planning
SB3463 alters ownership change rules for health care facilities in Illinois.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIFeb 5, 2026
FDA inspection citations: Ony Biotech, Inc. (3 observations)
FDA inspection raises concerns about drug quality at ONY Biotech.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIFeb 5, 2026
FDA inspection citations: NexCell Scientific Inc (13 observations)
FDA cites NexCell Scientific for multiple quality control issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORMSGLP-1 CompoundingFeb 3, 2026
MS SB2544: Mississippi Active Pharmaceutical Ingredient Quality Assurance Act; enact to impose certain provisions for compounding.
Mississippi compounding-ingredient quality bill; died in committee.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIFeb 3, 2026
FDA inspection citations: Iso-Tex Diagnostics, Inc. (5 observations)
FDA cites Iso-Tex Diagnostics for quality and sterility issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIJan 30, 2026
FDA inspection citations: Element Materials Technology Oakland-Concord (6 observations)
FDA cites facility for quality issues impacting compounded products.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIJan 30, 2026
FDA inspection citations: Hibrow Healthcare Private Limited (2 observations)
FDA cites facility for drug quality concerns; verify your suppliers.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIJan 29, 2026
FDA inspection citations: American Regent, Inc. (4 observations)
FDA inspection reveals citations at American Regent, Inc.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORHIGLP-1 CompoundingJan 28, 2026
HI SB3195: Relating To Drugs For Weight Loss.
HI SB3195 mandates coverage for GLP-1 weight loss drugs.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDAesthetic DevicesJan 28, 2026
FDA device recall (Class II): Brand Name: Leaseir Product Name: Leaseir Mhr Xcell Model/Catalog Number: Mhr 110-b Software Version: 1.5.0.0 Product D…
Leaseir MHR Xcell laser recalled for safety issues.
What to do — members only.Become a member →FDA Device Recallprimary source ↗ - MONITORMAMulti-topicJan 27, 2026
MA H5087: Regulating the operation of medical spas
Proposed Massachusetts med spa bill; superseded by a new draft, H5455.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingJan 22, 2026
FDA inspection citations: Anika Therapeutics, Inc. (4 observations)
FDA cites Anika Therapeutics for quality and sterility issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIJan 22, 2026
FDA inspection citations: Excel Vision (11 observations)
FDA cites Excel Vision for sterility and quality issues in inspection.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORIAScope of PracticeJan 20, 2026
IA HSB591: A bill for an act establishing the medical spa oversight Act, and making penalties applicable.
Proposed Iowa Medical Spa Oversight Act, with penalties.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIJan 9, 2026
FDA inspection citations: OneBlood, Inc. (1 observation)
FDA cites OneBlood for sterile compounding issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - CRITICALFEDGLP-1 CompoundingJan 7, 2026
FDA recall (Class II): Wegovy (Semaglutide) Injection, 0.5 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880…
FDA recalls Wegovy; med spas must check supplies.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIJan 7, 2026
FDA inspection citations: South Bend Medical Foundation, Inc. (1 observation)
FDA cites facility for sterile preparation issues impacting compounding.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingJan 7, 2026
FDA recall (Class II): Wegovy (Semaglutide) Injection, 1 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880 B…
FDA recalls Wegovy due to safety concerns; med spas must act.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIDec 22, 2025
FDA inspection citations: Blaine Labs Inc (12 observations)
FDA cites Blaine Labs for quality issues; med spas should verify sourcing.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIDec 19, 2025
FDA inspection citations: International Medication Systems Ltd. (8 observations)
FDA cites facility for sterility issues affecting med spas.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDMulti-topicDec 18, 2025
Primary Source Monitoring: Doctor Indicted for Orchestrating $45M Botox Fraud Scheme Targeting Medicare
Doctor indicted in $45M Botox fraud scheme targeting Medicare.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIDec 17, 2025
FDA inspection citations: Wyeth Pharmaceutical Division of Wyeth Holdings LLC (4 observations)
FDA cites Wyeth for sterility issues; verify your sourcing.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIDec 16, 2025
FDA inspection citations: Bello Bio LLC (13 observations)
FDA cites Bello Bio LLC for multiple sterile production violations.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORPAScope of PracticeDec 16, 2025
PA HB1881: Further providing for pharmacy technician and pharmacy technician trainee registration, qualifications and supervision; providing for administration of injectable medications, biologicals and immunizations, for clinical laboratory certificate and for report on pharmacy-administered vaccines; and making a repeal.
PA bill may expand pharmacy technicians' role in injectables.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDScope of PracticeDec 12, 2025
Primary Source Monitoring: Med Spa Owner Agrees to Plead Guilty to Performing Illegal Injections Using Unapproved Prescription Drugs
Legal repercussions for med spas using unapproved injection drugs.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIDec 12, 2025
FDA inspection citations: Greer Laboratories, Inc. (2 observations)
FDA cites Greer Laboratories for drug quality issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIDec 11, 2025
FDA inspection citations: Life Science Outsourcing, Inc. (5 observations)
FDA cites facility for serious sterile product issues; verify sourcing.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIDec 11, 2025
FDA inspection citations: Nubratori, Inc (3 observations)
FDA cites Nubratori, Inc. for sterile drug production issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIDec 11, 2025
FDA inspection citations: Denver Solutions, LLC (7 observations)
FDA cites Denver Solutions for compliance issues impacting med spas.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIDec 10, 2025
FDA inspection citations: Piramal Pharma Solutions Inc. (4 observations)
Med spas should verify sourcing from cited facility Piramal Pharma.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIDec 10, 2025
FDA inspection citations: Medtronic, Inc. (2 observations)
Important FDA citations for a facility impacting med spas.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIDec 9, 2025
FDA inspection citations: Biomat USA Inc (4 observations)
FDA cites Biomat USA for critical sterile production issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIDec 5, 2025
FDA inspection citations: Ecolab LLC (2 observations)
FDA cites Ecolab for drug product quality concerns; check your sources.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIDec 4, 2025
FDA inspection citations: St Mary's Medical Park Pharmacy (7 observations)
FDA cites compounding pharmacy for numerous quality issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDScope of PracticeDec 3, 2025
Primary Source Monitoring: Southern New Mexico Medical Spa Operator Settles Allegations of Controlled-Substance Recordkeeping Violations
Med spa operator faces penalties for recordkeeping violations.
What to do — members only.Become a member →Primary Source Monitoringprimary source ↗ - MONITORNHScope of PracticeDec 1, 2025
NH HB1321: Relative to the regulation of the provision of elective intravenous therapy.
Elective IV therapy regulation bill deemed inexpedient to legislate.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingNov 24, 2025
FDA / Federal Register Notice: Agency Information Collection Activities; Proposed Collection; Comment Request; Human Drug Compounding Under Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act
FDA seeks comments on human drug compounding practices.
What to do — members only.Become a member →Federal Registerprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAINov 21, 2025
FDA inspection citations: Sato Pharmaceutical Co., Ltd. (10 observations)
FDA cites Sato Pharmaceutical for quality concerns.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAINov 21, 2025
FDA inspection citations: Eagle Analytical Services, Inc. (4 observations)
Check sourcing from Eagle Analytical for sterile product compliance.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAINov 12, 2025
FDA inspection citations: Fordoz Pharma Co. (9 observations)
FDA cites Fordoz Pharma for sterile product issues; check your supply.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAINov 7, 2025
FDA inspection citations: Alliance Medical Products, Inc. (4 observations)
FDA cites facility for critical sterile product quality issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingNov 5, 2025
FDA recall (Class II): Semaglutide Injection, 10 mg/4 mL (2.5 mg/mL), 4mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Je…
FDA recalls Semaglutide injection over sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - CAUTIONFEDGLP-1 CompoundingNov 5, 2025
FDA recall (Class II): Semaglutide Injection, 2.5mg/1mL (2.5 mg/mL), 1mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jef…
Urgent: FDA recalls compounded semaglutide injection.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingNov 5, 2025
FDA recall (Class II): Semaglutide Injection, 5 mg/2 mL (2.5 mg/mL), 2mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jef…
FDA recalls GLP-1 product; take immediate action.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingNov 5, 2025
FDA recall (Class II): Semaglutide Injection, 6mg/2.4mL (2.5 mg/mL), 2.4mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 J…
FDA recalls Semaglutide injection due to sterility concerns.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingNov 5, 2025
FDA recall (Class II): Tirzepatide Injection, 27 mg/3 mL (9 mg/mL), 3mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeff…
Urgent FDA recall of Tirzepatide Injection impacts med spas.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAINov 5, 2025
FDA inspection citations: Fresenius Kabi Compounding, LLC (7 observations)
FDA cites compounding facility for quality and sterility issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingNov 5, 2025
FDA recall (Class II): Semaglutide Injection, 12.5/5mL (2.5 mg/mL), 5mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeff…
FDA recalls GLP-1 injection over sterility concerns.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingNov 5, 2025
FDA recall (Class II): Semaglutide Injection, 8mg/3.2mL (2.5 mg/mL), 3.2mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 J…
FDA recalls Semaglutide injection due to sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAINov 4, 2025
FDA inspection citations: Grand River Aseptic Manufacturing, Inc. (2 observations)
FDA cites Grand River Aseptic for concerns; verify your sourcing.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAINov 3, 2025
FDA inspection citations: Jubilant HollisterStier General Partnership (9 observations)
FDA cites facility for sterile drug production deficiencies.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIOct 20, 2025
FDA inspection citations: Par Health USA, LLC (4 observations)
FDA cites Par Health USA for serious sterile drug observations.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORPAScope of PracticeOct 17, 2025
PA SB1055: Further providing for pharmacy technician and pharmacy technician trainee registration, qualifications and supervision; providing for administration of injectable medications, biologicals and immunizations, for clinical laboratory certificate and for report on pharmacy-administered vaccines; and making a repeal.
PA's SB1055 could change injectable practice for pharmacy techs.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingOct 15, 2025
FDA recall (Class II): Semaglutide for Injection, a) 20 mg b) 20 mg/mL, 10 mL Multi-Dose Vials, GenoGenix, LLC, 2840 Nw 2nd Ave Ste 204 Boca R…
FDA recalls semaglutide over sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingOct 15, 2025
FDA recall (Class II): Semaglutide with B12 for Injection, all strengths and presentations, GenoGenix, LLC, 2840 Nw 2nd Ave Ste 204 Boca Raton…
FDA recalls GLP-1 product over sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingOct 15, 2025
FDA recall (Class II): Tirzepatide, 60mg/10 mL for Injection, 10mL vial lyophilized, all presentations, GenoGenix, LLC, 2840 Nw 2nd Ave Ste 20…
Important FDA recall on GLP-1 compounded product.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAISep 26, 2025
FDA inspection citations: Alcami Carolinas Corporation (3 observations)
FDA cites Alcami facility for quality control issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAISep 19, 2025
FDA inspection citations: Actavis Laboratories Ut, Inc. (4 observations)
FDA cites facility for sterility issues impacting compounded products.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAISep 19, 2025
FDA inspection citations: Barbara Ann Karmanos Cancer Hospital (3 observations)
FDA cites Karmanos Cancer Hospital for sterility and QA issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - CRITICALFEDGLP-1 CompoundingSep 10, 2025
FDA recall (Class II): Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy
FDA recalls compounded GLP-1 product for being subpotent.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingSep 10, 2025
FDA recall (Class II): Semaglutide, 2.5 mg/mL injection, 0.8 mL, Boothwyn Pharmacy
Class II recall of Boothwyn Pharmacy semaglutide injection (subpotent).
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingSep 10, 2025
FDA recall (Class II): Semaglutide, 2.5 mg/mL injection, 4 mL, Boothwyn Pharmacy
Urgent: GLP-1 injection recall for med spas sourcing compounded products.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAISep 5, 2025
FDA inspection citations: North American Custom Laboratories, LLC DBA FarmaKeio Superior Custom Compounding (1 observation)
FDA cites compounding facility for sterility issues; verify sources.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIAug 29, 2025
FDA inspection citations: Bio-Medical Pharmaceutical Manufacturing Corporation (9 observations)
FDA cites facility for issues affecting product quality and sterility.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIAug 22, 2025
FDA inspection citations: Nephron Sc, LLC (6 observations)
FDA cites Nephron SC for sterile drug production issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIAug 22, 2025
FDA inspection citations: Lonza Tampa LLC (9 observations)
FDA cites Lonza Tampa for multiple quality control issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIAug 15, 2025
FDA inspection citations: United Laboratories Manufacturing, LLC (8 observations)
FDA cites facility for quality issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORILLasers/EnergyAug 15, 2025
IL HB3248: Ins Cd-laser Hair Removal
Illinois requires insurance to cover laser hair removal from 2027.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Tirzepatide + Niacinamide 13.2 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, …
FDA recalls compounded GLP-1 product due to processing controls issue.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - CRITICALFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Steri…
FDA recalls compounded GLP-1 product.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Semaglutide + Cyanocobalamin injection solution, 2.21 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) s…
Stay informed: GLP-1 injectable recall may affect your practice.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Tirzepatide + Niacinamide 8.8 mg + 1.0mg/0.5 ml Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2…
Important recall of GLP-1 compounded product.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - CRITICALFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Tirzepatide + Niacinamide 16.6 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, …
Important recall for GLP-1 products; take immediate action.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Tirzepatide + Niacinamide 11.24 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile,…
FDA recalls compounded GLP-1 product over safety issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Tirzepatide + Niacinamide 4.4 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2…
FDA recalls a GLP-1 product; check your supply immediately.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Tirzepatide + Niacinamide 2.2 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2…
FDA recalls compounded GLP-1 product due to safety concerns.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Semaglutide + Cyanocobalamin 0.88 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Steri…
Ongoing recall of compounded GLP-1 product.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Semaglutide + Cyanocobalamin 0.22 mg + 0.25mg/0.5 ml Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Steri…
Alert: GLP-1 product recall due to processing issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Semaglutide + Cyanocobalamin 0.44 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Steri…
Important recall for compounded GLP-1 products impacts med spas.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Tirzepatide + Niacinamide 6.6 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2…
Important FDA recall for compounded GLP-1 product impacts med spas.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingAug 13, 2025
FDA recall (Class II): Semaglutide +Cyanocobalamin 1.5 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile…
FDA recalls compounded GLP-1 product.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIAug 12, 2025
FDA inspection citations: Fareva Morton Grove, Inc. (7 observations)
FDA cites concerns at Fareva Morton Grove; check your product sources.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIAug 8, 2025
FDA inspection citations: Steri-Pharma, LLC (3 observations)
FDA cites Steri-Pharma for quality concerns; verify your sources.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIJul 31, 2025
FDA inspection citations: Telix IsoTherapeutics Group, Inc. (10 observations)
FDA cites Telix for multiple sterile production issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIJul 31, 2025
FDA inspection citations: Cardinal Health 414, LLC (5 observations)
FDA cites Cardinal Health for sterility and quality issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingJul 30, 2025
FDA / Federal Register Notice: Outsourcing Facility Fee Rates for Fiscal Year 2026
FDA fees for outsourcing facilities impact compounding.
What to do — members only.Become a member →Federal Registerprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIJul 28, 2025
FDA inspection citations: Doh Central Pharmacy (6 observations)
FDA cites DOH Central Pharmacy for quality and sterility issues.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIJul 24, 2025
FDA inspection citations: North American Science Associates, LLC (1 observation)
FDA inspection raises concerns over product sterility.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIJul 18, 2025
FDA inspection citations: Right Value Drug Stores LLC (5 observations)
Inspecting citations may impact med spa sources for injectables.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: OAIJul 16, 2025
FDA inspection citations: Bso LLC (9 observations)
FDA cites BSO LLC for concerns impacting sterile drug quality.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingFDA: VAIJul 15, 2025
FDA inspection citations: Biomat Holdings Mount Vernon Newark (1 observation)
FDA cites facility for contamination issues; verify your sources.
What to do — members only.Become a member →FDA Inspection Citationprimary source ↗ - MONITORFEDGLP-1 CompoundingJul 2, 2025
FDA recall (Class II): Tirzepatide/Cyanocobalamin Injectable, 15mg/1mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, S…
Class II recall of Thrive Health tirzepatide/B12 over sterility.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingJul 2, 2025
FDA recall (Class II): Tirzepatide/Cyanocobalamin Injectable, 30mg/1mg/mL (15mg/0.5mg/0.5mL), pre-filled syringe, Thrive Health Solutions, 88 …
FDA recalls GLP-1 product due to sterility concerns.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - CRITICALFEDGLP-1 CompoundingJul 2, 2025
FDA recall (Class II): Tirzepatide Injections, 30mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewo…
FDA recalls Tirzepatide injections; action needed.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingJul 2, 2025
FDA recall (Class II): Tirzepatide Injections, 20mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewo…
FDA recalls Tirzepatide for sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingJul 2, 2025
FDA recall (Class II): Semaglutide/Cyanocobalamin Injectable, 5mg/1mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Su…
FDA recalls compounded GLP-1 product for sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - CRITICALFEDGLP-1 CompoundingJul 2, 2025
FDA recall (Class II): Semaglutide, 2.5 mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, Co 80…
FDA recalls GLP-1 product over sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingJul 2, 2025
FDA recall (Class II): Semaglutide, 5 mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, Co 80112
FDA recalls compounded GLP-1 product over sterility issues.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORFEDGLP-1 CompoundingJul 2, 2025
FDA recall (Class II): Tirzepatide Injections, 10mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewo…
Class II recall of Thrive Health tirzepatide over sterility concerns.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITOROHLasers/EnergyJul 1, 2025
OH SB226: Regards use of light-based medical devices for hair removal
Proposed Ohio rules on light-based devices for hair removal.
What to do — members only.Become a member →LegiScanprimary source ↗ - CAUTIONRINATIONALScope of PracticeJun 30, 2025
RI H5351: Mandates cosmetic medical procedures be performed by a physician, PA, APRN, or delegated to a qualified non-physician, non-PA or non-APRN under the supervision of a physician, physician assistant, or advanced practice registered nurse.
Major changes in who can perform cosmetic procedures in RI med spas.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORRIScope of PracticeJun 30, 2025
RI S0976: Mandates cosmetic medical procedures be performed by a physician, PA, APRN, or delegated to a qualified non-physician, non-PA or non-APRN under the supervision of a physician, physician assistant, or advanced practice registered nurse.
RI law mandates supervision for cosmetic procedures
What to do — members only.Become a member →LegiScanprimary source ↗ - CAUTIONTXNATIONALScope of PracticeJun 20, 2025
TX HB3749: Relating to the regulation of the provision of elective intravenous therapy.
Texas HB 3749 regulates elective IV therapy; effective Sept 1, 2025.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORTXScope of PracticeMay 15, 2025
TX SB2696: Relating to the regulation of the performance of cosmetic injections; requiring an occupational certificate; authorizing fees.
Certification required for cosmetic injectors in Texas by 2026.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORTXNeuromodulatorsMay 8, 2025
TX SB1117: Relating to the administration of botulinum toxin by dentists.
TX SB1117 allows dentists to inject botulinum toxin by 2025.
What to do — members only.Become a member →LegiScanprimary source ↗ - CRITICALFEDGLP-1 CompoundingMay 7, 2025
FDA recall (Class II): Wegovy (Semaglutide) injection, 2.4 mg/0.75 mL, 4 Single-Dose Prefilled Pens per Carton, For Subcutaneous Use Only, Rx …
Urgent recall of Wegovy due to temperature abuse risks.
What to do — members only.Become a member →FDA Enforcementprimary source ↗ - MONITORMEMulti-topicMay 6, 2025
ME LD1374: An Act to Establish Additional Requirements for Dentists to Administer Botulinum Toxin and Dermal Fillers
LD1374 proposing dentist regulations on toxins and fillers is dead.
What to do — members only.Become a member →LegiScanprimary source ↗ - CAUTIONCOScope of PracticeApr 7, 2025
CO HB1024: Medical-Aesthetic Services Delegation Disclosures
Disclosure requirements for delegating medical-aesthetic services.
What to do — members only.Become a member →LegiScanprimary source ↗ - MONITORFEDGLP-1 Compounding
FDA / Federal Register Notice: Agency Information Collection Activities; Proposed Collection; Comment Request; Registration of Human Drug Compounding Outsourcing Facilities Under the Federal Food, Drug, and Cosmetic Act and Associated Fees
Registration requirements for drug compounding facilities proposed.
What to do — members only.Become a member →Federal Registerprimary source ↗
Browse the full archive → Every material change on record, grouped by year — including changes older than the 18 months shown above.