Stryker Corporation 2025-01-29 Health serious FDA
Health · FDA · Recall #FDA-Z-0981-2025
stryker 3.0MM Neuro Match Head, REF 5820-107-430, used to cut bone and bone cement during… Recall
Issued January 29, 2025 · Stryker Corporation
In January 2025, Stryker Corporation recalled the stryker 3.0MM Neuro Match Head, REF 5820-107-430, used to cut bone and bone cement during…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).
What you should do
- 1 Stop using stryker 3.0MM Neuro Match Head, REF 5820-107-430, used to cut bone and bone cement during… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Stryker Corporation 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
- Stryker Corporation
- Category
- Health
- Recall date
- January 29, 2025
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of UK, Netherlands, New Zealand.
- Recall number
- FDA-Z-0981-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Stryker Corporation has 15 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.