BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2222913 · Received July 15, 2011

    Report

    Report Number
    1824206-2011-03756
    Event Type
    Malfunction
    Date Received
    July 15, 2011
    Date of Event
    June 30, 2011
    Report Date
    July 1, 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

    TECH FOUND THE STRETCHER IN THE BASEMENT. LEFT END TUBE WAS BROKEN CAUSING THE SIDERAIL NOT TO LATCH. REPLACED THE END TUBE TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINANT RECEIVED THAT THE SIDERAIL WOULD NOT LATCH. NO INJURY ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. P8000

    Patients

    Seq Age Sex Outcome Treatment
    1