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Olympus Corporation of the Americas recalls Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2
Recalled July 26, 2023 · FDA recall Z-2012-2023 · Olympus Corporation of the Americas
Hazard
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope. · FDA Class I
Units
4 units
Sold at
US Nationwide Distribution.
Description
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Product
Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →