Class II

Medical Device Recall: 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

ConMed Corporation · July 14, 2026

Reason for Recall

Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.

Distribution

US Nationwide distribution in the state of TX.

States Affected

NATIONWIDE

Quantity Affected

2 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3018-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

ConMed Corporation Medical Device Recall: 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 | SafeCheck