Drug recall
Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.
FDA recall event 77223 · Class II · Zimmer Biomet, Inc.
Key facts
| Event ID | 77223 |
|---|---|
| Recall numbers | Z-2198-2017 |
| Recalling firm | Zimmer Biomet, Inc. |
| Product type | Devices |
| Products | Reusable instruments in the Knee, Hip, Trauma, and Extremities segments. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Durability characteristics of reusable instruments were not established |
| Initiation date | May 8, 2017 |
| Report date | Jun 7, 2017 |
| Termination date | Dec 1, 2017 |
| 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: