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Recall Observatory FDA recall evidence

Device product

Olympus Tracheal Intubation Fiberscope, Models LF-P & LF-V.

Z-2501-2023

July 27, 2023

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 92779
Status
Ongoing
Classification
Class II
Quantity
2127 units
Official record key
device-enforcement:Z-2501-2023

Official wording

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

Code information: UDI-DI: 04953170051098, 04953170452932, & 04953170156250; 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.