Home / Recalls / Medical Devices
Synthes USA HQ, Inc. recalls Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur fractures.
Recalled December 4, 2013 · FDA recall Z-0409-2014 · Synthes USA HQ
Hazard
The Synthes 4.5 mm LCP Curved Condylar Plate was recalled because a Straight Condylar Plate is etched with a Curved Condylar Plate part number. · FDA Class II
Units
13
Sold at
Worldwide Distribution - USA including ID, FL, TN, NY, LA and Internationally to Canada.
Description
The Synthes 4.5 mm LCP Curved Condylar Plate was recalled because a Straight Condylar Plate is etched with a Curved Condylar Plate part number.
Product
Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur fractures.
Manufacturer(s)
Synthes USA HQ, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →