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Olympus Corporation of the Americas recalls Olympus EVIS EXERA II BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-P180, BF-Q180, BF-Q180-AC, BF-1T180, BF-1TQ180
Recalled July 26, 2023 · FDA recall Z-2016-2023 · Olympus Corporation of the Americas
Hazard
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope. · FDA Class I
Units
17,609 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 II BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-P180, BF-Q180, BF-Q180-AC, BF-1T180, BF-1TQ180
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →