Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Blueprint Software Recalled by Tornier S.A.S. Due to The software bug allows for case planning with...
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 Software, Catalog #BPUE001.
Why Was This Recalled?
The software bug allows for case planning with anatomic glenoid Perform / Perform Augmented implants and anatomic humeral Tornier Flex implant configurations that are incompatible and do not have regulatory approval.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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