BEUDAMED
    FDA Recall Completed

    Discovery NM/CT 670 Pro, model 5376204-70-54

    Recall: Z-0608-2019 · Initiated May 24, 2018

    Recall

    Recall Number
    Z-0608-2019
    Event Number
    81680
    Firm
    GE Healthcare, LLC
    FEI Number
    2126677
    Product Code
    KPS
    Status
    Completed
    Root Cause
    Component change control
    Initiated
    May 24, 2018
    Address
    3000 N Grandview Blvd, Waukesha, WI, 53188-1615

    Description

    Discovery NM/CT 670 Pro, model 5376204-70-54

    Reason

    When your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) (outside of the A1 panel) may not have been wired correctly which could result in these not shutting off all power to the entire system as intended, resulting in a potential electric hazard.

    Action

    The firm initiated the recall by letter on 05/24/2018. The letter explained the issue and requested the UPS(s) be disconnected from the system until the system could be repaired.

    Distribution

    CA, DC, OH, UT, WI, Canada

    Quantity

    1 unit