Home / Recalls / Medical Devices
Olympus Corporation of the Americas recalls Bronchofiberscope BF-XP60
Recalled October 10, 2018 · FDA recall Z-3307-2018 · 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
1296
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
Bronchofiberscope BF-XP60
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →