BEUDAMED
    FDA Enforcement Class I Ongoing

    Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75, 0998-UC-0800-75, 0998-00-0800-83, 0998-UC-0800-83, 0998-00-0800-85, 0998-UC-0800-85.

    Recall: Z-0337-2022 · Reported December 22, 2021

    Enforcement

    Recall Number
    Z-0337-2022
    Event ID
    88983
    Classification
    Class I
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Datascope Corp.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    December 22, 2021
    Initiation Date
    November 15, 2021
    Classification Date
    December 15, 2021
    Address
    1300 Macarthur Blvd, Mahwah, NJ, 07430-2052, United States

    Description

    Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75, 0998-UC-0800-75, 0998-00-0800-83, 0998-UC-0800-83, 0998-00-0800-85, 0998-UC-0800-85.

    Reason

    Firm is initiating a correction due to the possibility of fluid ingress. Fluid entering the device may short various electronic components thus leading to system shutdown, which could result in unsafe hemodynamic instability.

    Code Info

    All Serial Numbers. May also be designated as part number D998 etc. Model Number, UDI-DI: 0998-00-0800-75, 10607567112312; 0998-UC-0800-75, 10607567112312; 0998-00-0800-83, 10607567108407; 0998-UC-0800-83, 10607567108407; 0998-00-0800-85, 10607567113449; 0998-UC-0800-85, 10607567113449.

    Distribution

    Worldwide distribution - US Nationwide.

    Quantity

    44 (US); 5 (OUS)