BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2012906 · Received March 4, 2011

    Report

    Report Number
    1824206-2011-01267
    Event Type
    Malfunction
    Date Received
    March 4, 2011
    Date of Event
    February 10, 2011
    Report Date
    February 10, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE LEFT GAS SPRING WAS LEAKING HYDRAULIC FLUID AND THE RIGHT GAS SPRING WAS SLIGHTLY BENT. HE REPLACED BOTH HEAD GAS SPRINGS TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE HEAD SECTION WOULD NOT GO ALL THE WAY DOWN TO A FLAT SURFACE.

    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