Tornier S.A.S. 2025-04-16 Health serious FDA
Health · FDA · Recall #FDA-Z-1535-2025
stryker Blueprint Mixed Reality Glenoid Digitizer, Catalog Number MRUE201, packaged in… Recall
Issued April 16, 2025 · Tornier S.A.S.
In April 2025, Tornier S.A.S. recalled the stryker Blueprint Mixed Reality Glenoid Digitizer, Catalog Number MRUE201, packaged in…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
What you should do
- 1 Stop using stryker Blueprint Mixed Reality Glenoid Digitizer, Catalog Number MRUE201, packaged in… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Tornier S.A.S. 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
- Tornier S.A.S.
- Category
- Health
- Recall date
- April 16, 2025
- Units affected
- Not reported
- Sold at
- US: TX, MN, AK, PA, MA, TN, ID, and France, Canada, and Ireland
- Recall number
- FDA-Z-1535-2025
- Made in
- France
- Issuing agency
- FDA
In context
- Tornier S.A.S. has 2 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.