Home / Recalls / Medical Devices
Aesculap, Inc. recalls Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
Recalled March 6, 2013 · FDA recall Z-0887-2013 · Aesculap
Hazard
The bipolar energy did not stop after release of the foot pedal. · FDA Class II
Units
59
Sold at
USA Nationwide Distribution including the states of: AR, CA, FL, IN, IA, KS, MD, MN, MO, OR, TN, TX, VA and WA.
Description
The bipolar energy did not stop after release of the foot pedal.
Product
Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
Manufacturer(s)
Aesculap, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →