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 changed & why it matters
Med Spa Radar recorded an FDA device recall at the federal level, dated January 28, 2026, in the Aesthetic Devices category.
A recall 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 Device Recall
- Jurisdiction
- Federal
- Category
- Aesthetic Devices
- Recorded
- January 28, 2026
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
Free weekly Brief
Get the changes that matter in plain English, every week — and be alerted when the rules move. No charge.
Members get the full “what to do” on every alert — in real time, for your states. Become a member →
FDA Device Recall · primary source ↗
Monitoring, not legal advice.