Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
G7 Acetabular System Recalled by Biomet, Inc. Due to The outer package labeling and product etch are...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Biomet, Inc. directly.
Affected Products
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
Quantity: 12 units
Why Was This 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.
Where Was This Sold?
This product was distributed to 6 states: AZ, FL, GA, MI, NE, TX
About Biomet, Inc.
Biomet, Inc. has 250 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report