Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker CLAW II ORTHOLOC 3DSi Plate Recalled by Wright Medical Technology Inc Due to The incorrect product is contained in the packaging.
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
Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
Quantity: 23 units
Why Was This Recalled?
The incorrect product is contained in the packaging.
Where Was This Sold?
This product was distributed to 7 states: AZ, ID, IA, NY, NC, VA, WV
About Wright Medical Technology Inc
Wright Medical Technology Inc has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report