medical MODERATE Updated 2026-09-02

ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposabl

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Recalled 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

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI:10845854042472, Lot number 1513167

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

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View official government recall

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