Home / Recalls / Olympus Corporation of the Americas / Z-0191-2024

Z-0191-2024 Class I Ongoing

Recalled by Olympus Corporation of the Americas — Center Valley, PA

Recall Details

Product Type
Devices
Report Date
November 15, 2023
Initiation Date
October 12, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
13950 devices

Product Description

EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Numbers BF-1T180, BF-1TQ180, BF-P180

Reason for Recall

There is a risk of endobronchial combustion if high-frequency cauterization is performed while supplying oxygen [and/or] the electrode section of the electrosurgical accessory is too close to the distal end of the endoscope.

Distribution Pattern

US Nationwide distribution

Code Information

Model BF-1T180 UDI-DI: N/A; Model BF-1TQ180 UDI-DI: N/A; Model BF-P180 UDI-DI: N/A;

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