GENESYS Cross FT Suture Anchor with Two #2 — Class II medical device recall Z-1619-2013
Terminated recall by Linvatec Corp. dba ConMed Linvatec, reported 2013-07-10, distributed in FL, KY, LA, MI, NC, NY. Incorrect blue/white suture was used.
| Recall number | Z-1619-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec, Largo, FL, United States |
| Recall initiated | 2013-03-06 |
| Classified | 2013-07-01 |
| Reported by FDA | 2013-07-10 |
| Terminated | 2013-07-22 |
| Distributed | FL, KY, LA, MI, NC, NY |
| Quantity | 60 units |
| Lot numbers | 431437 |
| Model numbers | CFBC-4502 |
Product
GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Hi-FI Registered Trade Mark Sutures Rx Only STERILE EO CONMED LINVATEC REF CFBC-4502. Reattachment of soft tissue to bone in orthopedic surgical procedures
Reason for recall
Incorrect blue/white suture was used.
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-1619-2013. 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.