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; take action!
What changed & why it matters
Med Spa Radar recorded an FDA enforcement action at the federal level, dated November 5, 2025, in the GLP-1 Compounding category, naming Semaglutide.
A recall of Semaglutide is a supply-chain event, not a rule that might change: if the pharmacy or outsourcing facility a med spa sources from distributed an affected lot, it is a patient-safety and liability exposure today. Recalls are the clearest signal that a supplier a practice may already use has a quality problem on record with the FDA.
- Type
- FDA Enforcement
- Jurisdiction
- Federal
- Category
- GLP-1 Compounding
- Substance
- Semaglutide
- Recorded
- November 5, 2025
What this means for your specific practice — the exact step to take, the deadline to calendar, or the supplier detail to check — is in the member "what to do" below. This page is the free record of what changed and why it matters.
What to do
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FDA Enforcement · primary source ↗
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Monitoring, not legal advice.