Biomet, Inc. 2024-05-01 Health serious FDA
Health · FDA · Recall #FDA-Z-1607-2024
Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082.… Recall
Issued May 1, 2024 · Biomet, Inc.
In May 2024, Biomet, Inc. recalled the Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082.…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Possible damage to the Vanguard Knee System AS Tibial Bearing caused during the manufacturing process.
What you should do
- 1 Stop using Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082.… 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
- May 1, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide in the state of IN and the countries of Canada, India, Netherlands, and P.R. China.
- Recall number
- FDA-Z-1607-2024
- 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 737th Health recall we've logged in 2024.