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Olympus Corporation of the Americas recalls Olympus EVIS EXERA III BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-H190, BF-Q190, BF-XT190, BF-1TH190
Recalled July 26, 2023 · FDA recall Z-2017-2023 · Olympus Corporation of the Americas
Hazard
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope. · FDA Class I
Units
9,684 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 III BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-H190, BF-Q190, BF-XT190, BF-1TH190
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →