Drug recall
The 2nd Assist Knee Positioner
FDA recall event 79141 · Class II · Zimmer Biomet, Inc.
Key facts
| Event ID | 79141 |
|---|---|
| Recall numbers | Z-0803-2018 |
| Recalling firm | Zimmer Biomet, Inc. |
| Product type | Devices |
| Products | The 2nd Assist Knee Positioner |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution. |
| Initiation date | Sep 7, 2017 |
| Report date | Mar 7, 2018 |
| Termination date | Aug 23, 2018 |
| 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: