Drug recall
Biomet 20mm Compress Device Short Anchor Plug With Drill Set / With Pin Inserter Ion Implant Item number…
FDA recall event 81513 · Class II · Zimmer Biomet, Inc.
Key facts
| Event ID | 81513 |
|---|---|
| Recall numbers | Z-0553-2019 |
| Recalling firm | Zimmer Biomet, Inc. |
| Product type | Devices |
| Products | Biomet 20mm Compress Device Short Anchor Plug With Drill Set / With Pin Inserter Ion Implant Item number: 178562 Product Usage: 1. Correction of revision of unsuccessful osteotomy, arthrodesis, or… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential metal burrs in the holes of the device preventing the appropriate drill and transverse pins from being inserted |
| Initiation date | Oct 24, 2018 |
| Report date | Dec 12, 2018 |
| Termination date | Apr 14, 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: