Home / Recalls / Olympus Corporation of the Americas / Z-2504-2023

Z-2504-2023 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
10801 units

Product Description

Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP.

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: 04953170136856, 04953170340192, 04953170061998, 04953170340215, 04953170317576, & 04953170136825; All Serial Numbers.

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