On Feb 2, 2026, this item appeared in the FDA’s recall database under a product area that overlaps with medical aesthetics.
Why recalls matter to a med spa. A recall doesn’t always mean a product is dangerous — it can range from a labeling correction to a genuine safety removal. But it’s exactly the kind of thing that’s easy to miss and expensive to ignore. If a device, injectable, or product on your shelf is involved, you want to know before a client does.
What to do right now:
Check whether this product, device, or lot is anything you currently stock or use.
If it is, stop using the affected lots and set them aside until you’ve confirmed the scope.
Pull the official recall notice (linked below) for the exact lot numbers, dates, and the recall classification (Class I/II/III).
Contact your distributor or the manufacturer for return, replacement, or corrective-action instructions.
Document what you found and what you did — a one-line note in your records is cheap insurance.
Read the official FDA record for the full details, affected lots, and recall reason.
View the official FDA record ↗
This post summarizes a public FDA database entry for medical-aesthetics owners. It is general business information, not medical, legal, or regulatory advice. Always confirm scope, lot numbers, and classification against the official FDA record, and consult your own clinician or counsel for anything clinical or compliance-related.