Drug recall
OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of…
FDA recall event 91423 · Class II · Biomet, Inc.
Key facts
| Event ID | 91423 |
|---|---|
| Recall numbers | Z-1036-2023 |
| Recalling firm | Biomet, Inc. |
| Product type | Devices |
| Products | OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee Item… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement |
| Initiation date | Nov 29, 2022 |
| Report date | Feb 8, 2023 |
| City | Warsaw |
| State | IN |
| Country | United States |
| FEI number | 1825034 |
At a glance
- 1–9 Products in this recall
- None 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: