Drug recall
Persona Partial Knee Spacer Blocks To assist in partial knee arthroplasty surgery
FDA recall event 79395 · Class II · Zimmer Biomet, Inc.
Key facts
| Event ID | 79395 |
|---|---|
| Recall numbers | Z-1240-2018 |
| Recalling firm | Zimmer Biomet, Inc. |
| Product type | Devices |
| Products | Persona Partial Knee Spacer Blocks To assist in partial knee arthroplasty surgery |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Zimmer Biomet is conducting a medical device recall for the Persona Partial Knee Spacer Blocks in sizes 8mm, 9mm, 10mm, 12mm, and 14mm. Complaints received indicated that flexion has the potential to… |
| Initiation date | Oct 24, 2017 |
| Report date | Apr 4, 2018 |
| Termination date | Apr 3, 2019 |
| 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: