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Olympus Corporation of the Americas recalls BF-1TQ180: EVIS EXERA II Bronchovideoscope
Recalled May 18, 2022 · FDA recall Z-1049-2022 · Olympus Corporation of the Americas
Hazard
Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization · FDA Class II
Units
242 units
Sold at
US Nationwide distribution.
Description
Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization
Product
BF-1TQ180: EVIS EXERA II Bronchovideoscope
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →