Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate Recalled by Tornier, Inc Due to One lot of Tournier Perform Reversed Lateralized Baseplates...
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 Reversed Augmented Glenoid Lateralized Baseplate, 25mm, Offset +3mm, REF DWJ502
Quantity: 30 units
Why Was This Recalled?
One lot of Tournier Perform Reversed Lateralized Baseplates were found to have been manufactured with 6mm spacers instead of 3mm spacers. This nonconformance prevents the central screw from being able to thread into the baseplate.
Where Was This Sold?
This product was distributed to 10 states: CA, CO, IL, MA, MN, NC, OR, RI, SC, TN
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