Z-3018-2026 Class II Ongoing
FDA device recall Z-3018-2026 was initiated by ConMed Corporation on July 14, 2026 and is designated Class II. Reason for recall: Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability. The recall status is ongoing. Affected quantity: 2 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 2, 2026
- Initiation Date
- July 14, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2 units
Product Description
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 Pattern
US Nationwide distribution in the state of TX.
Code Information
UDI:10845854042472, Lot number 1513167