BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRAUMA TRANSTAR

    MDR report key: 2253799 · Received August 10, 2011

    Report

    Report Number
    1824206-2011-04195
    Event Type
    Malfunction
    Date Received
    August 10, 2011
    Date of Event
    July 28, 2011
    Report Date
    July 28, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THE BED IN HALL. SIDERAIL WOULD NOT LATCH. SIDERAIL END TUBE WAS BENT CAUSING SIDERAIL NOT TO LATCH. REPLACED SIDERAIL END TUBE TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

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

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRAUMA TRANSTAR WHEELED STRETCHER FPO HILL-ROM, INC. P8040

    Patients

    Seq Age Sex Outcome Treatment
    1