BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2220499 · Received July 18, 2011

    Report

    Report Number
    1824206-2011-03793
    Event Type
    Malfunction
    Date Received
    July 18, 2011
    Date of Event
    June 30, 2011
    Report Date
    June 30, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN REPLACED THE SIDERAIL END TUBE TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE SIDERAIL WILL NOT LATCH DUE TO A BROKEN RIGHT SIDERAIL END TUBE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. 8005

    Patients

    Seq Age Sex Outcome Treatment
    1