CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B... recall (ConMed Corporation)
Medical deviceClass IIOngoing
Summary: ConMed Corporation is recalling 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. Reason: Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
What is 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
Why
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the state of TX. (states named: Texas)
How to tell if yours is affected
UDI:10845854042472, Lot number 1513167
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-3018-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | July 14, 2026 |
| Reported | September 2, 2026 |
| Company | ConMed Corporation |
| Company location | Utica, NY, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 2 units |
More recalls from ConMed Corporation · all medical device recalls · recalls from July 2026