FDA Device recall Z-1284-2023
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
- FDA Device
- Class II
- ongoing
- Published 2023-03-29
On 2023-03-29 the FDA classified a Class II recall of G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462 by Biomet, citing the outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1284-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-02-06 |
| Published | 2023-03-29 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Biomet |
| Distribution | AZ, FL, GA, MI, NE, TX |
Product
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
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.
Identifiers
| code_info | UDI: (01)00880304703506(17)321128(10)65731960; Lot Number: 65731960 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1284-2023%22
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