BEUDAMED
    FDA Recall Open, Classified

    Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment

    Recall: Z-1629-2023 · Initiated February 17, 2023

    Recall

    Recall Number
    Z-1629-2023
    Event Number
    92175
    Firm
    Arjohuntleigh Magog, Inc.
    FEI Number
    3002655016
    Product Code
    FSA
    Status
    Open, Classified
    Root Cause
    Process control
    Initiated
    February 17, 2023
    Posted
    May 24, 2023
    Address
    2001 Tanguay St, Magog Canada

    Description

    Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment

    Reason

    Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.

    Action

    Arjo issue an URGENT MEDICAL DEVICE RECALL notice to its consignees on 02/17/2023 via letter, UPS, 2nd Day Delivery. The notice explained the problem, the risk, and requested the consignee remove the units from use and destroy them. The firm will be replacing the units upon receipt of the completed response form. For questions or assistance in completing the Customer Response Form, please contact Arjo at 1 800-323-1245 or via email at [email protected].

    Distribution

    US: OH, NY

    Quantity

    3