BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3150309 · Received May 30, 2013

    Report

    Report Number
    1824206-2013-02911
    Event Type
    Malfunction
    Date Received
    May 30, 2013
    Date of Event
    May 3, 2013
    Report Date
    May 3, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT FOUND THE SIDE RAIL IS BROKEN AND THE END TUBE IS NOT CONNECTED TO TOP OF THE SIDE RAIL BECAUSE THE RATCHET RIVETS ARE MISSING. THE ACCOUNT REPLACED THE SIDE RAIL RATCHET RIVETS TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE SIDE RAIL IS NOT LATCHING. NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    237997 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1