Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DELTA XTEND" Reverse Shoulder System Modular Centered and Eccentric Epiphysis Recalled by DePuy Orthopaedics, Inc. Due to The affected lots are being recalled because the...
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
DELTA XTEND" Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants are intended for use in total shoulder or hemi-shoulder replacement procedures in patients with non-functional rotator cuffs. HA components are for cementless use only.
Quantity: 23,053 units
Why Was This Recalled?
The affected lots are being recalled because the epiphysis may not assemble to the stem, which may cause a surgical delay.
Where Was This Sold?
Nationally
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