Home / Recalls / Medical Devices
Olympus Corporation of the Americas recalls High Frequency Resection Electrodes, endoscope, ac-powered and accessories The electrodes are used for endoscopic diagn
Recalled July 5, 2017 · FDA recall Z-2629-2017 · Olympus Corporation of the Americas
Hazard
Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes. · FDA Class II
Units
1264 units
Sold at
Nationwide Distribution
Description
Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes.
Product
High Frequency Resection Electrodes, endoscope, ac-powered and accessories The electrodes are used for endoscopic diagnosis and treatment in urological and gynecological applications.
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →