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Synthes, Inc. recalls Stem Extractor f/Guide Bar, Part number 03.401.072. Instrumentation for extraction and revision of Epoca shoulder impla
Recalled May 2, 2018 · FDA recall Z-1514-2018 · Synthes
Hazard
There is a potential for the connection screw of the stem extractor to break. · FDA Class II
Units
31
Sold at
Worldwide Distribution: US (nationwide) and to countries of: Canada and Switzerland.
Description
There is a potential for the connection screw of the stem extractor to break.
Product
Stem Extractor f/Guide Bar, Part number 03.401.072. Instrumentation for extraction and revision of Epoca shoulder implants.
Manufacturer(s)
Synthes, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →