Recall archive / FDA device enforcement
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462 — FDA record Z-1284-2023
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Feb 6, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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.
- Classification
- Class II
- Recalling firm
- Biomet, Inc.
- Quantity
- 12 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1284-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI: (01)00880304703506(17)321128(10)65731960; Lot Number: 65731960 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US Distribution to states of: AZ, FL, GA, MI, NE, and TX.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Mar 29, 2023
- Recall initiation date
- Feb 6, 2023
- Center classification date
- Mar 23, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.