BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1062158 · Received June 13, 2008

    Report

    Report Number
    1824206-2008-02667
    Event Type
    Malfunction
    Date Received
    June 13, 2008
    Date of Event
    April 11, 2008
    Report Date
    April 11, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MS, 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 TECH REPLACED THE BASE FRAME IN ORDER TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    THE WELD FAILED ON THE PT LEFT CASTER TUBE ON THE BASE FRAME OF THIS STRETCHER. THERE WAS NO INDICATION OF PT INVOLVEMENT.

    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