G7 Acetabular System — Class II medical device recall Z-1284-2023
Ongoing recall by Biomet, Inc., reported 2023-03-29, distributed in AZ, FL, GA, MI, NE, TX. The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C l
| Recall number | Z-1284-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2023-02-06 |
| Classified | 2023-03-23 |
| Reported by FDA | 2023-03-29 |
| Distributed | AZ, FL, GA, MI, NE, TX |
| Quantity | 12 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00880304703506 |
| Lot numbers | 65731960 |
| Model numbers | 110024462 |
Product
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
Reason for recall
The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1284-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.