BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2031761 · Received March 21, 2011

    Report

    Report Number
    1824206-2011-01720
    Event Type
    Malfunction
    Date Received
    March 21, 2011
    Date of Event
    March 2, 2011
    Report Date
    March 2, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT THE HEAD SECTION WILL NOT RAISE OR LOWER DUE TO BROKEN GAS SPRING ON HEAD SECTION ASSEMBLY. REPLACED THE BROKEN GAS SPRING TO RESOLVE THIS ISSUE. BED FOUND ON 6TH FLOOR.

    Description of Event or Problem · 1

    COMPLAINANT RECEIVED THAT ALLEGED THE HEAD SECTION WILL NOT RAISE OR LOWER. NO PATIENT IMPACT.

    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