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Olympus Corporation of the Americas recalls Airway Mobilescope MAF-TM
Recalled October 10, 2018 · FDA recall Z-3311-2018 · Olympus Corporation of the Americas
Hazard
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port. · FDA Class II
Units
3456
Sold at
The products were distributed US nationwide and Canada.
Description
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
Product
Airway Mobilescope MAF-TM
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →