United StatesCONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF CFBC-5502B, 5.5 mm, supplied sterile with two #2 (5 metric) Hi‑Fi sutures (UDI 10845854042472, Lot 1513167), sold in Texas (2 units), is affected. It was recalled because the suture anchor may contain an incorrect patient implant card, which may result in incorrect device identification and traceability.
What's being recalled
CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anchor with two, #2 (5 metric) Hi-Fi Sutures Sterile
Recalling firm: ConMed Corporation, Utica, NY, United States.
How to identify it
UDI:10845854042472, Lot number 1513167
The hazard
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the state of TX.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)
Canada