Drug recall
TRABECULAR METAL MODULAR ACETABULAR SYSTEM, Shell with Cluster Holes, Porous 60mm. Catalog number…
FDA recall event 67795 · Class II · Zimmer, Inc.
Key facts
| Event ID | 67795 |
|---|---|
| Recall numbers | Z-1496-2014 |
| Recalling firm | Zimmer, Inc. |
| Product type | Devices |
| Products | TRABECULAR METAL MODULAR ACETABULAR SYSTEM, Shell with Cluster Holes, Porous 60mm. Catalog number 00-6202-060-22; Hip implant component. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The shell was missing the locking ring. |
| Initiation date | Apr 1, 2014 |
| Report date | Apr 30, 2014 |
| Termination date | Sep 11, 2014 |
| City | Warsaw |
| State | IN |
| Country | United States |
| FEI number | 1000220733 |
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: