Home / Recalls / Medical Devices
Synthes, Inc. recalls Synthes 3.2 mm Guide Wire 400mm. Used for guiding the TFN Helical Blade and TFN Lag Screw into the femoral.
Recalled February 26, 2014 · FDA recall Z-0986-2014 · Synthes
Hazard
Synthes 3.2 mm Guide Wire 400mm included an incorrect raw material listed on the label. · FDA Class II
Units
1,132,096
Sold at
Worldwide Distribution-USA (nationwide) and the countries of Canada and Switzerland.
Description
Synthes 3.2 mm Guide Wire 400mm included an incorrect raw material listed on the label.
Product
Synthes 3.2 mm Guide Wire 400mm. Used for guiding the TFN Helical Blade and TFN Lag Screw into the femoral.
Manufacturer(s)
Synthes, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →