BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRAUMA TRANSTAR STRETCHER

    MDR report key: 2053466 · Received March 17, 2011

    Report

    Report Number
    1824206-2011-01650
    Event Type
    Malfunction
    Date Received
    March 17, 2011
    Date of Event
    February 21, 2011
    Report Date
    February 21, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE LOWER PIVOT BOLT WAS MISSING FROM THE SIDERAIL LATCH. THE TECHNICIAN REPLACED THE BOLT TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE SIDERAIL IS BROKEN AND WILL NOT LATCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRAUMA TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8040

    Patients

    Seq Age Sex Outcome Treatment
    1