BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRETCHER

    MDR report key: 1853031 · Received September 21, 2010

    Report

    Report Number
    1831750-2010-02467
    Event Type
    Malfunction
    Date Received
    September 21, 2010
    Date of Event
    August 24, 2010
    Report Date
    August 24, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT, THE HYDRAULICS WERE NOT WORKING PROPERLY. IT WAS REPORTED THE HEAD END HYDRAULICS WOULD CONTINUE TO LOWER AFTER THE RELEASE PEDALS STOPPED BEING ACTIVATED. THERE WAS NO PT INVOLVEMENT. NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV 1010 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA