BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1070836 · Received July 3, 2008

    Report

    Report Number
    1824206-2008-02787
    Event Type
    Malfunction
    Date Received
    July 3, 2008
    Date of Event
    June 21, 2008
    Report Date
    June 21, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UPON COMPLAINT REVIEW, IT WAS DETERMINED THAT IT IS A REPORTABLE EVENT FOR SIDERAIL NOT LATCHING. THE TECHNICIAN REPLACED VARIOUS SIDERAIL HARDWARE IN ORDER TO RESOLVE THE PROBLEM.

    Description of Event or Problem · 1

    SIDERAILS WOULD NOT LATCH ON THIS STRETCHER.

    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