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Medacta Usa recalls GMK Intramedullary Extension Rod 100 mm is a rod to obtain correct leg alignment during total knee replacement. Rod to
Recalled November 19, 2014 · FDA recall Z-0202-2015 · Medacta Usa
Hazard
Medacta has registered in its database 3 cases of breakage of the GMK Intramedullary Extension Rod 100 mm, code 02.07.10.0162. · FDA Class II
Units
1 rod (US); 145 rods (global)
Sold at
Worldwide Distribution - US including OH and Internationally to Australia, Austria, Belgium, France, Germany, Greece, Italy, Japan, Portugal, South Africa, Spain, and Switzerland.
Description
Medacta has registered in its database 3 cases of breakage of the GMK Intramedullary Extension Rod 100 mm, code 02.07.10.0162.
Product
GMK Intramedullary Extension Rod 100 mm is a rod to obtain correct leg alignment during total knee replacement. Rod to obtain correct leg alignment during total knee replacement.
Manufacturer(s)
Medacta Usa
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →