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Olympus Corporation of the Americas recalls Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
Recalled August 1, 2018 · FDA recall Z-2518-2018 · Olympus Corporation of the Americas
Hazard
Potential breakage of the endoscope s insertion tube bending section during surgical procedures · FDA Class II
Units
2548
Sold at
US Nationwide and Canada
Description
Potential breakage of the endoscope s insertion tube bending section during surgical procedures
Product
Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →