Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RSP Glenoid Baseplate Recalled by Encore Medical, LP Due to Coating hex did not engage with the Straight...
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
RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.
Quantity: 146 units
Why Was This Recalled?
Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver
Where Was This Sold?
This product was distributed to 17 states: AZ, CA, FL, IN, KS, KY, ME, MN, MS, NJ, OH, RI, SC, TN, TX, VA, WA
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