BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2113018 · Received May 25, 2011

    Report

    Report Number
    1824206-2011-02894
    Event Type
    Malfunction
    Date Received
    May 25, 2011
    Date of Event
    May 5, 2011
    Report Date
    May 5, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THE PATIENT RIGHT SIDERAIL WAS NOT LATCHING, AS THE END TUBE WAS BROKEN. REPLACED THE LATCH END TUBE. TUBE BROKEN DUE TO ABUSE. STRETCHED WAS FOUND IN BASEMENT REPAIR AREA.

    Description of Event or Problem · 1

    COMPLAINT RECEIVED INDICATED THAT THE SIDERAIL WAS BROKEN. 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