FDA recall Z-3018-2026

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 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.

Key facts

Status

Ongoing

Initiation date

2026-07-14

Report date

2026-09-02

Voluntary/Mandated

Voluntary: Firm initiated

Location

Utica, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3018-2026