Drug recall
Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
FDA recall event 71850 · Class II · Biomet, Inc.
Key facts
| Event ID | 71850 |
|---|---|
| Recall numbers | Z-2483-2015 |
| Recalling firm | Biomet, Inc. |
| Product type | Devices |
| Products | Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The device was assembled without screw hole plugs. |
| Initiation date | Jul 28, 2015 |
| Report date | Sep 9, 2015 |
| Termination date | May 17, 2016 |
| 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: