Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ORTHOLOC 3DSi CLAW II 4 HOLE Plate Recalled by Wright Medical Technology, Inc. Due to Stryker has identified an issue that impacts two...
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 Wright Medical Technology, Inc. directly.
Affected Products
ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone fixation device
Quantity: 10 units
Why Was This Recalled?
Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for 402S0425 incorrectly contained 40241425, and vice versa.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Wright Medical Technology, Inc.
Wright Medical Technology, Inc. has 69 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report