Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
stryker Blueprint Mixed Reality Glenoid Digitizer Recalled by Tornier S.A.S. Due to Stryker identified an elevated complaint rate related to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Tornier S.A.S. directly.
Affected Products
stryker Blueprint Mixed Reality Glenoid Digitizer, Catalog Number MRUE201, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty
Quantity: 22 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 7 states: AK, ID, MA, MN, PA, TN, TX
About Tornier S.A.S.
Tornier S.A.S. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report