Drug recall
Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty
FDA recall event 79250 · Class II · Zimmer Biomet, Inc.
Key facts
| Event ID | 79250 |
|---|---|
| Recall numbers | Z-1011-2018 |
| Recalling firm | Zimmer Biomet, Inc. |
| Product type | Devices |
| Products | Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The affected products are labeled as a 62.5mm LEFT Femur; however, the contents are a Vanguard 70mm RIGHT Femur. |
| Initiation date | Oct 3, 2017 |
| Report date | Mar 21, 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: