BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2133784 · Received May 12, 2011

    Report

    Report Number
    1824206-2011-02688
    Event Type
    Malfunction
    Date Received
    May 12, 2011
    Date of Event
    April 20, 2011
    Report Date
    April 20, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN ISOLATED THE ISSUE TO THE FOOT HYDRAULIC CYLINDER RELEASE. HE REPLACED FOOT CYLINDER TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE STRETCHER WILL NOT GO INTO REVERSE TRENDELENBURG.

    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