BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2011965 · Received February 14, 2011

    Report

    Report Number
    1824206-2011-00819
    Event Type
    Malfunction
    Date Received
    February 14, 2011
    Date of Event
    January 20, 2011
    Report Date
    January 20, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE HEAD PIN BOLT WAS MISSING FROM THE LINKAGE AT THE FOOT OF THE STRETCHER. HE REPLACED THE HEAD PIN BOLT AND SECURED THE LINKAGE AT HEAD AS WELL.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE TIRES ARE ROTATING WHILE THE UNIT IS IN BRAKE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1