Biomet, Inc. Recall 91866
Description: G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
Biomet, Inc. Recall 91866 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-1284-2023 |
| Event ID | 91866 |
| Event Description | G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462 |
| Product Type | Devices |
| Distribution | US Distribution to states of: AZ, FL, GA, MI, NE, and TX. |
| Quantity | 12 units |
| Recall Reason | The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner. |
| Device Classification | 20230329 |
| Device Code Info | UDI: (01)00880304703506(17)321128(10)65731960; Lot Number: 65731960 |
| Center Classification Date | 20230323 |
| Recall Initiation Date | 20230206 |
| Recalling Firm | Biomet, Inc. |
| Initial Notification | Letter |
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