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Encore Medical, Lp recalls Turon Impaction Fixture

Recalled March 15, 2017 · FDA recall Z-1412-2017 · Encore Medical

Hazard
During the Turon 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. · FDA Class II
Units
297 units
Sold at
US, South Korea, Australia, Canada, United Kingdom/Ireland, Germany

Description

During the Turon 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.

Product
Turon Impaction Fixture
Manufacturer(s)
Encore Medical, Lp

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Encore Medical, Lp recalls Turon Impaction Fixture | RecallWatchUSA