Synthes (USA) Products LLC 2024-03-13 Health serious FDA
Health · FDA · Recall #FDA-Z-1242-2024
Opal, Intervertebral Cage, 10x32mm, h 11mm, Revolvable-Indicated for degenerative spine… Recall
Issued March 13, 2024 · Synthes (USA) Products LLC
In March 2024, Synthes (USA) Products LLC recalled the Opal, Intervertebral Cage, 10x32mm, h 11mm, Revolvable-Indicated for degenerative spine…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Products not sterilized, sterility cannot be confirmed
What you should do
- 1 Stop using Opal, Intervertebral Cage, 10x32mm, h 11mm, Revolvable-Indicated for degenerative spine… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Synthes (USA) Products LLC 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
- Synthes (USA) Products LLC
- Category
- Health
- Recall date
- March 13, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Argentina, Austria, Australia, Belgium, Canada, Czech Republic, Germany, Spain,
- Recall number
- FDA-Z-1242-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Synthes (USA) Products LLC has 5 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.