Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ATTUNE Revision CRS Femoral RT SZ 5 Cemented Recalled by DePuy Orthopaedics, Inc. Due to There may be burrs on the extraction hole...
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 CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Implant, Knee
Quantity: 1 unit
Why Was This Recalled?
There may be burrs on the extraction hole threads.
Where Was This Sold?
This product was distributed to 3 states: FL, MO, PA
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