Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Tornier Perform Humeral System Recalled by Tornier, Inc Due to Devices from one lot of Perform" Reversed Inserts...
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, Inc directly.
Affected Products
Stryker Tornier Perform Humeral System, Reversed Insert, 45%, REF DWP2393, for shoulder arthroplasty
Quantity: 38 units
Why Was This Recalled?
Devices from one lot of Perform" Reversed Inserts may contain a locking ring that was assembled upside down which would prevent the humeral insert from securely seating in the stem or spacer.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Tornier, Inc
Tornier, Inc has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report