PlainRecalls
FDA Devices Critical Class I Ongoing

Olympus BRONCHOVIDEOSCOPE, Model Numbers BF-Q170

Reported: July 26, 2023 Initiated: June 8, 2023 #Z-2015-2023

Product Description

Olympus BRONCHOVIDEOSCOPE, Model Numbers BF-Q170

Reason for Recall

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Details

Units Affected
1 units
Distribution
US Nationwide Distribution.
Location
Center Valley, PA

Frequently Asked Questions

What product was recalled?
Olympus BRONCHOVIDEOSCOPE, Model Numbers BF-Q170. Recalled by Olympus Corporation of the Americas. Units affected: 1 units.
Why was this product recalled?
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 26, 2023. Severity: Critical. Recall number: Z-2015-2023.