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Recall Observatory FDA recall evidence

Device product

Olympus Bronchovideoscope, Models BF-1T180, BF-1TQ180, BF-P180, & BF-Q180.

Z-2493-2023

July 27, 2023

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 92779
Status
Ongoing
Classification
Class II
Quantity
3652 units
Official record key
device-enforcement:Z-2493-2023

Official wording

Reason: Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.

Code information: UDI-DI: 04953170308215, 04953170288975, 04953170339325, 04953170308222, 04953170289002, 04953170339349, 04953170308192, 04953170317965, 04953170339288, 04953170288883, 04953170308208, 04953170288937; All Serial Numbers.

Distribution pattern: US Nationwide distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.