FDA recall Z-0686-2024

Shirakawa Olympus Co., Ltd. · Class II · device

Product

Model No. BF-P190, EVIS EXERA III Bronchovideoscope

Reason for recall

Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.

Distribution

US Nationwide distribution.

Key facts

Status
Ongoing
Initiation date
2023-12-04
Report date
2024-01-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Nishishirakawa-Gun, Japan

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0686-2024