BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRYKER

    MDR report key: 1011236 · Received February 15, 2008

    Report

    Report Number
    1011236
    Event Type
    Malfunction
    Date Received
    February 15, 2008
    Date of Event
    February 14, 2008
    Report Date
    February 15, 2008
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US

    Narratives

    Description of Event or Problem · 1

    NURSES WENT TO LIFT PATIENT. PLACED HEAD OF THE GURNEY IN THE FLAT POSITION USING THE SIDE RAIL BUTTON AND LIFTED THE PATIENT. NURSES USED SIDE RAIL BUTTON TO LIFT HEAD OF THE GURNEY HIGHER, AND THE HEAD OF THE GURNEY WOULD NOT GO UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER STRETCHER, BED FPO STRYKER MEDICAL 1550 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *