BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2094037 · Received April 20, 2011

    Report

    Report Number
    1824206-2011-02309
    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
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE HEAD PANEL SECTION STUCK IN THE UP POSITION AND THE GAS SPRING CYLINDER WAS LEAKING FLUID. HE REPLACED THE GAS SPRING TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE HEAD PANEL SECTION WILL NOT LOWER.

    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