BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO AMBULANCE COT

    MDR report key: 1875036 · Received October 13, 2010

    Report

    Report Number
    1831750-2010-02790
    Event Type
    Malfunction
    Date Received
    October 13, 2010
    Date of Event
    September 15, 2010
    Report Date
    September 15, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE BEYOND EXPECTED SERVICE LIFE. DEVICE FAILURE DUE TO EXCESSIVE AGE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE CARRIAGE WILL NOT RAISE BACK UP. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO AMBULANCE COT STRETCHER, WHEELED FPO STRYKER CORP., MEDICAL DIV 6080 NA

    Patients

    Seq Age Sex Outcome Treatment
    1