Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM Recalled by Wright Medical Technology, Inc. Due to Plates manufactured from an incorrect raw material.
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
CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM, REF 40S20020, 1 EACH, Rx ONLY, NON STERILE Orthopedic
Quantity: 0
Why Was This Recalled?
Plates manufactured from an incorrect raw material.
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