Z-2499-2023 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
122 units

Product Description

Olympus Airway Mobilescope, Models MAF-DM2, MAF-GM2, & MAF-TM2.

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: 04953170407260, 04953170407208, and 04953170407147; All Serial Numbers.