Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee Recalled by DePuy Orthopaedics, Inc. Due to Packaging may include screws that are not intended...
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 Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001
Quantity: 10 units
Why Was This Recalled?
Packaging may include screws that are not intended to be used with the 5mm augments, may cause delay in surgery
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