Biomet, Inc. 2023-03-29 Health serious FDA
Health · FDA · Recall #FDA-Z-1284-2023
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number… Recall
Issued March 29, 2023 · Biomet, Inc.
In March 2023, Biomet, Inc. recalled the G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
What you should do
- 1 Stop using G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Biomet, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Biomet, Inc.
- Category
- Health
- Recall date
- March 29, 2023
- Units affected
- Not reported
- Sold at
- US Distribution to states of: AZ, FL, GA, MI, NE, and TX.
- Recall number
- FDA-Z-1284-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Biomet, Inc. has 6 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.