Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AltiVate Reverse Small Socket Insert Recalled by Encore Medical, LP Due to Mislabeling
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 Encore Medical, LP directly.
Affected Products
AltiVate Reverse Small Socket Insert, 44mm Semi Constrained - E-Plus, Part Number: 509-03-044 - Product Usage: Per IFU, DJO Surgical shoulder devices are intended for treatment of patients who are candidates for shoulder arthroplasty per the Indication for use.
Quantity: 15
Why Was This Recalled?
Product mislabeled. Use may result in a delay in surgery, stopping of surgery, and revision surgery.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Encore Medical, LP
Encore Medical, LP has 54 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report