FDA-Device2018-10-10Class II
Bronchofibercope BF-6C240
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.
Sold states
The products were distributed US nationwide and Canada.
Affected count
197
Manufactured in
3500 Corporate Pkwy, PO Box 610, Center Valley, PA, United States
Products
Bronchofibercope BF-6C240
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3293-2018Don't want to check this manually?
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