Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD) Recalled by DePuy Orthopaedics, Inc. Due to There is the potential for debris/material to be...
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 DePuy Orthopaedics, Inc. directly.
Affected Products
CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.
Quantity: 12639 total
Why Was This Recalled?
There is the potential for debris/material to be found behind the O-rings in the neck trials.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About DePuy Orthopaedics, Inc.
DePuy Orthopaedics, Inc. has 154 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report