BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1900625 · Received November 8, 2010

    Report

    Report Number
    1824206-2010-10919
    Event Type
    Malfunction
    Date Received
    November 8, 2010
    Date of Event
    October 13, 2010
    Report Date
    October 13, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ID, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT FOUND THE CYLINDER WAS DEFECTIVE. THE ACCOUNT REPLACED THE HEAD HI/LOW CYLINDER TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD HI/LOW CYLINDER IS NOT HOLDING THE WEIGHT AFTER INSTALL. THE HEAD HI/LOW DRIFTS DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1