BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1062236 · Received June 17, 2008

    Report

    Report Number
    1824206-2008-02690
    Event Type
    Malfunction
    Date Received
    June 17, 2008
    Date of Event
    April 17, 2008
    Report Date
    April 17, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UPON COMPLAINT REVIEW, IT WAS DETERMINED THAT THIS CONDITION HAS THE POTENTIAL TO CAUSE SERIOUS INJURY WERE IT TO REOCCUR, THE TECHNICIAN REPLACED THE BASE FRAME IN ORDER TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    THE WELD FAILED ON THE CASTER TUBE ON THE BASE FRAME OF THIS STRETCHER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM RITTER P8005 NA

    Patients

    Seq Age Sex Outcome Treatment
    1