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Olympus Corporation of the Americas recalls Uretero-reno fiberscope URF-P6RP6
Recalled August 1, 2018 · FDA recall Z-2520-2018 · Olympus Corporation of the Americas
Hazard
Breakage of the endoscope's insertion tube bending section during surgical procedures. · FDA Class II
Units
2399
Sold at
US Nationwide. Canada and Mexico
Description
Breakage of the endoscope's insertion tube bending section during surgical procedures.
Product
Uretero-reno fiberscope URF-P6RP6
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →