Conmed Corporation: Fastener, Fixation, Biodegradable, Soft Tissue
Recall Summary ConMed Corporation is recalling GENESYS CrossFT Suture Anchors (model CFBC-5502B) distributed nationwide because some units may have an incorrect patient implant card included, which could cause confusion about device identification and tracking. This is a Class II recall affecting medical devices used in soft tissue fixation procedures. The affected products were distributed across all U.S. states and Washington, D.C.
- Recalling firm
- ConMed Corporation
- 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
- Reason
- Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-07-14
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the state of TX.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/4a5b53e4-a193-4288-a56e-d3e07704a048