Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115. The Recalled by DePuy Orthopaedics, Inc. Due to The device will not connect to the Specialist...
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
SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115. The product is a femoral cutting block.
Quantity: 140 total units
Why Was This Recalled?
The device will not connect to the Specialist 2 Locating Outrigger which renders them unusable in surgery.
Where Was This Sold?
This product was distributed to 5 states: IA, MA, NY, OH, 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