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Biomet, Inc. recalls G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
Recalled March 29, 2023 · FDA recall Z-1284-2023 · Biomet
Hazard
The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner. · FDA Class II
Units
12 units
Sold at
US Distribution to states of: AZ, FL, GA, MI, NE, and TX.
Description
The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
Product
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →