Home / Recalls / Olympus Corporation of the Americas / Z-2501-2023

Z-2501-2023 Class II Ongoing

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

Recall Details

Product Type
Devices
Report Date
September 6, 2023
Initiation Date
July 27, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2127 units

Product Description

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

Reason for Recall

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

Distribution Pattern

US Nationwide distribution.

Code Information

UDI-DI: 04953170051098, 04953170452932, & 04953170156250; All Serial Numbers.

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