Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Reverse Shoulder Prosthesis Stem Impaction Fixture REF 804-03-053 The Turon Recalled by Encore Medical, Lp Due to During the assembly, the impaction forces caused 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 Encore Medical, Lp directly.
Affected Products
Reverse Shoulder Prosthesis Stem Impaction Fixture REF 804-03-053 The Turon and RSP Impaction Fixtures are used in the operating room on the back table to assemble the shoulder systems for implant. The Turon Fixture is used to connect the Humeral Head to the Humeral Neck, then subsequently to assemble the Humeral Stem to the Head/Neck construct. The RSP Fixture is used to assemble the UHMWPE Socket Inserts to both the RSP Socket Shells and Monoblock Stems.
Quantity: 634 units
Why Was This Recalled?
During the assembly, the impaction forces caused the polymer, black acetal copolymer from the Impaction Fixture to wear off on the lateral surface of the Humeral Stem titanium plasma spray coating.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Encore Medical, Lp
Encore Medical, Lp has 43 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report