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Smith & Nephew, Inc. recalls TRIGEN, Intramedullary nail - Product Usage: is intended to provide resistance for screw back-out. It provides additiona
Recalled July 29, 2020 · FDA recall Z-2685-2020 · Smith & Nephew
Hazard
A manufacturing error which resulted in the re-sterilization of the ultra-high-molecular-weight polyethylene (UHMWPE) sleeve. · FDA Class II
Units
12 units
Sold at
International distribution in the countries of Brazil, Colombia and United Arab Emirates.
Description
A manufacturing error which resulted in the re-sterilization of the ultra-high-molecular-weight polyethylene (UHMWPE) sleeve.
Product
TRIGEN, Intramedullary nail - Product Usage: is intended to provide resistance for screw back-out. It provides additional friction to help hold the screws in place.
Manufacturer(s)
Smith & Nephew, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →