Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ATTUNE REVISION CEMENTED STEM 16X80MM-intended for use in total knee Recalled by DePuy Orthopaedics, Inc. Due to Package labeled as 16mm x 80mm contained a...
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
ATTUNE REVISION CEMENTED STEM 16X80MM-intended for use in total knee arthroplasty Part Number: 1512-16-080
Quantity: 7 units
Why Was This Recalled?
Package labeled as 16mm x 80mm contained a 16mm x 130mm stem instead and result in obtaining a replacement
Where Was This Sold?
International distribution in the countries of Canada, France.
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