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Olympus Corporation of the Americas recalls Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE, Model Number BF-XT160
Recalled July 26, 2023 · FDA recall Z-2014-2023 · Olympus Corporation of the Americas
Hazard
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope. · FDA Class I
Units
284 units
Sold at
US Nationwide Distribution.
Description
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Product
Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE, Model Number BF-XT160
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →