Olympus Corporation of the Americas recalls BF-P180 EVIS EXERA II Bronchovideoscope, Model No. BF-P180
Recalled Product
BF-P180 EVIS EXERA II Bronchovideoscope, Model No. BF-P180
Hazard / Issue
The firm is issuing validated, new reprocessing instructions according to the FDA 2015 guidance, "Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling."
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: All serial numbers
View official government recall
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