BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1061775 · Received June 13, 2008

    Report

    Report Number
    1824206-2008-02651
    Event Type
    Malfunction
    Date Received
    June 13, 2008
    Date of Event
    May 22, 2008
    Report Date
    May 22, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE BRAKES NOT HOLDING LEAD TO UNINTENTIONAL MOVEMENT OF THE STRETCHER WHICH HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN COULD FIND NO PROBLEMS WITH THE BRAKING SYSTEM UPON INSPECTION, HE STATED THAT HE DID MAKE SOME ADJUSTMENTS TO THE BRAKES BUT COULD NOT DUPLICATE THE PROBLEM ORIGINALLY.

    Description of Event or Problem · 1

    NURSING STAFF REPORTED THAT WHILE THE STRETCHER BRAKES WERE LOCKED THE STRETCHER STARTED TO ROLL WITH A PATIENT ON IT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM RITTER P8000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1