Drug recall
G7 Acetabular Screw 6.5mmx35mm Part Number: 010001000
FDA recall event 66967 · Class II · Biomet, Inc.
Key facts
| Event ID | 66967 |
|---|---|
| Recall numbers | Z-0493-2014 |
| Recalling firm | Biomet, Inc. |
| Product type | Devices |
| Products | G7 Acetabular Screw 6.5mmx35mm Part Number: 010001000 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Investigation identified that the outer label, inner label, and patient label all have the incorrect diameter size of 10.5mm. The screw is actually a 6.5mm diameter and correctly corresponds to the… |
| Initiation date | Nov 26, 0013 |
| Report date | Jan 1, 2014 |
| Termination date | Sep 29, 2014 |
| 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: