BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO IT COT OBS

    MDR report key: 2800271 · Received October 8, 2012

    Report

    Report Number
    1831750-2012-10495
    Event Type
    Malfunction
    Date Received
    October 8, 2012
    Date of Event
    September 10, 2012
    Report Date
    September 10, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    HEIGHT ADJUSTMENT RACKS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEIGHT ADJUSTMENT RACKS WERE NOT LOCKING INTO POSITION PROPERLY. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO IT COT OBS WHEELED, STRETCHER FPO STRYKER MEDICAL 6081 NA

    Patients

    Seq Age Sex Outcome Treatment
    1