Biomet, Inc. 2023-11-29 Health serious FDA
Health · FDA · Recall #FDA-Z-0387-2024
Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful… Recall
Issued November 29, 2023 · Biomet, Inc.
In November 2023, Biomet, Inc. recalled the Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
What you should do
- 1 Stop using Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful… 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
- November 29, 2023
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, CANADA, CHILE, JAPAN, NETHERLANDS, NEW ZEALAND.
- Recall number
- FDA-Z-0387-2024
- 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 903rd Health recall we've logged in 2023.