Reported Mar 29, 2023 · Ongoing
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
Biomet, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
G7 Acetabular SystemDual Mobility Acetabular Liner40 mmSize DModel Number 110024462
- Lot codes and dates
- UDI(01)00880304703506(17)321128(10)65731960
- Lot Number65731960
- Amount recalled
- 12 units
Where it was sold
Why it was recalled
The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
This product could cause temporary or reversible health problems — stop using it.
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