Drug recall
Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764
FDA recall event 82004 · Class II · Zimmer Biomet, Inc.
Key facts
| Event ID | 82004 |
|---|---|
| Recall numbers | Z-0937-2019, Z-0938-2019 |
| Recalling firm | Zimmer Biomet, Inc. |
| Product type | Devices |
| Products | Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764, Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label. |
| Initiation date | Dec 21, 2018 |
| Report date | Mar 6, 2019 |
| Termination date | May 13, 2020 |
| 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: