Drug recall
GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Hi-FI Registered Trade Mark Sutures Rx Only STERILE EO…
FDA recall event 65166 · Class II · Linvatec Corp. dba ConMed Linvatec
Key facts
| Event ID | 65166 |
|---|---|
| Recall numbers | Z-1619-2013 |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect blue/white suture was used. |
| Initiation date | Mar 6, 2013 |
| Report date | Jul 10, 2013 |
| Termination date | Jul 22, 2013 |
| City | Largo |
| State | FL |
| Country | United States |
| FEI number | 1017294 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: