Official recall notice
FDA DeviceClass IINotable
FDA Recall: CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESY
- Recall date
- 2026-09-02
- Brand
- ConMed Corporation
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
Product description
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
Affected products
UDI:10845854042472, Lot number 1513167