BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1010548 · Received February 15, 2008

    Report

    Report Number
    1010548
    Event Type
    Malfunction
    Date Received
    February 15, 2008
    Date of Event
    February 13, 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

    WHEN HUSBAND OF THE PATIENT TRIED TO RAISE THE HEAD OF THE GURNEY, THE GURNEY MOTOR MECHANISM FAILED. THE GURNEY HEAD LOWERED ON ITS OWN.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *