BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OBGYN TRANSTAR STRETCHER

    MDR report key: 2094038 · Received April 20, 2011

    Report

    Report Number
    1824206-2011-02310
    Event Type
    Malfunction
    Date Received
    April 20, 2011
    Date of Event
    March 28, 2011
    Report Date
    March 28, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE CASTERS WERE RATCHETING AND WORN OUT. THE TECHNICIAN REPLACED THE CASTERS TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES ALL FOUR BRAKE CASTERS HAVE MOVEMENT/SWIVEL WHEN IN THE BRAKE POSITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OBGYN TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8050

    Patients

    Seq Age Sex Outcome Treatment
    1