FDAFDA · Food and drugs·Recall number Z-3018-2026
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
Published September 2, 2026 · Recall initiated: July 14, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- ConMed Corporation
- Distributor
- US Nationwide distribution in the state of TX.
- Lot
- UDI:10845854042472, Lot number 1513167
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.