GENESYS CrossFT Suture Anchor
ConMed recalls GENESYS CrossFT Suture Anchor (REF CFBC-5502B) due to incorrect implant card.
If you have a GENESYS CrossFT Suture Anchor with Disposable Driver (REF CFBC-5502B), check the patient implant card for accuracy and contact ConMed for further instructions.
Recall at a glance
- Quantity recalled
- 2 units
Why it was recalled
ConMed is recalling the GENESYS CrossFT Suture Anchor with Disposable Driver (REF CFBC-5502B) because the suture anchor may contain an incorrect patient implant card, which could result in incorrect device identification and traceability.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
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
- Lot code
- 1513167
- UDI-DI
- 10845854042472
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other Device Defect recalls
Other recent recalls from ConMed Corporation
Editorial summary by Recall Canary · summary updated 2026-08-27 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification