Drug recall
Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
FDA recall event 77022 · Class II · Biomet Microfixation, LLC
Key facts
| Event ID | 77022 |
|---|---|
| Recall numbers | Z-2073-2017 |
| Recalling firm | Biomet Microfixation, LLC |
| Product type | Devices |
| Products | Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Part of the number on the tray lid differ from the part number on the base. |
| Initiation date | Apr 11, 2017 |
| Report date | May 24, 2017 |
| Termination date | Aug 6, 2019 |
| City | Jacksonville |
| State | FL |
| Country | United States |
| FEI number | 1032347 |
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: