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ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anc
Recalled September 2, 2026 · FDA recall Z-3018-2026 · ConMed
Hazard
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability. · FDA Class II
Units
2 units
Sold at
US Nationwide distribution in the state of TX.
Description
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
Product
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
Manufacturer(s)
ConMed Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →