BEUDAMED
    FDA Enforcement Class II Ongoing

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

    Recall: Z-2499-2023 · Reported September 6, 2023

    Enforcement

    Recall Number
    Z-2499-2023
    Event ID
    92779
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Olympus Corporation of the Americas
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    September 6, 2023
    Initiation Date
    July 27, 2023
    Classification Date
    August 31, 2023
    Address
    3500 Corporate Pkwy, N/A, Center Valley, PA, 18034-8229, United States

    Description

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

    Reason

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

    Code Info

    UDI-DI: 04953170407260, 04953170407208, and 04953170407147; All Serial Numbers.

    Distribution

    US Nationwide distribution.

    Quantity

    122 units