ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.
- Recalling company
- 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 – may cause temporary or medically reversible health consequences
- Recall date
- Jul 14, 2026
- Reported
- Sep 2, 2026
- Distribution
- US Nationwide distribution in the state of TX.
- Status
- Ongoing
- Quantity
- 2 units
- Lot / codes
- UDI:10845854042472, Lot number 1513167
- Company location
- Utica, NY
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3018-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3018-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.