Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented Recalled by DePuy Orthopaedics, Inc. Due to Fifty (50) individual units from Lot D20111130 were...
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
DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented prosthesis. Part Number: 1365-21-000, Part Description: ARTICUL/EZE BALL 32 +1 GR
Quantity: 50 units
Why Was This Recalled?
Fifty (50) individual units from Lot D20111130 were distributed with the incorrect part number and size etched on the product.
Where Was This Sold?
This product was distributed to 21 states: CA, CT, FL, GA, IN, IA, LA, ME, MN, MO, MT, NE, NY, NC, OH, OK, OR, PA, SC, TN, WI
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