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US Endoscopy Group Inc recalls Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp, dis
Recalled October 7, 2015 · FDA recall Z-0001-2016 · US Endoscopy Group
Hazard
The company has determined the sterility cannot be assured for the affected lot. · FDA Class II
Units
41 units
Sold at
US Distribution to states of: AL, AR, CA, IL, IN, MS, OH, OK & TN.
Description
The company has determined the sterility cannot be assured for the affected lot.
Product
Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp, dissect and transect tissue during gastrointestinal endoscopic procedures.
Manufacturer(s)
US Endoscopy Group Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →