FDA-Device2026-09-02Class IIMISBRANDING
ConMed Linvatec GENESYS CrossFT Suture Anchor recalled for incorrect implant card
What this means
Some ConMed Linvatec GENESYS CrossFT Suture Anchors (REF# CFBC-5502B, Lot 1513167) may contain an incorrect patient implant card. This card is used to identify and track the device after implantation, so an incorrect card could lead to confusion about which device was used.
- Check implant records for Lot 1513167 (UDI: 10845854042472).
- Verify the patient implant card matches the actual device implanted.
- Contact ConMed Corporation if you have questions about affected units.
The agency's original wording
Hazard
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution in the state of TX.
Affected count
2 units
Manufactured in
525 French Rd, N/A, Utica, NY, United States
Products
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
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3018-2026Want us to check the next one for you?
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