Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Variable Angle Locking Compression Plate/VA-LCP Dorsal Distal Radius Plate Recalled by Synthes USA HQ, Inc. Due to It was discovered that one of the VA-LCP...
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 Synthes USA HQ, Inc. directly.
Affected Products
Variable Angle Locking Compression Plate/VA-LCP Dorsal Distal Radius Plate, Part Number 02.115.431. Indicated for: Dorsally displaced fractures, Open joint reconstruction, and Corrective osteotomies after distal radius malunion.
Quantity: 4
Why Was This Recalled?
It was discovered that one of the VA-LCP Dorsal Distal Radius Plates was incorrectly etched as Part Number 02.115.431 (110 degree) instead of the correct Part Number 02.115.231 (90 degree).
Where Was This Sold?
This product was distributed to 4 states: IN, OH, PA, TX
About Synthes USA HQ, Inc.
Synthes USA HQ, Inc. has 56 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report