CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver… — Class II medical device recall Z-3018-2026
Ongoing recall by ConMed Corporation, reported 2026-09-02, distributed nationwide. Suture anchor may contain incorrect patient implant card which may result in incorrect device identification a
| Recall number | Z-3018-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ConMed Corporation, Utica, NY, United States |
| Recall initiated | 2026-07-14 |
| Classified | 2026-08-26 |
| Reported by FDA | 2026-09-02 |
| Distributed | Nationwide (US) |
| Quantity | 2 units |
| UPC / GTIN / UDI-DI | 10845854042472 |
| Lot numbers | 1513167 |
| Model numbers | 5.5MM, CFBC-5502B |
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
Reason for recall
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3018-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.