CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Su… recall
ConMed Corporation recalled CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Su… on September 2, 2026 because of suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability. It was sold nationwide.
Why it was recalled
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
What's recalled
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
Quantity: 2 units
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- ConMed Corporation, Utica, NY
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide distribution in the state of TX. - Status
- Ongoing
- Recall number
- Z-3018-2026
- Source
- U.S. Food and Drug Administration
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