BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 2222471 · Received July 13, 2011

    Report

    Report Number
    1831750-2011-07023
    Event Type
    Malfunction
    Date Received
    July 13, 2011
    Date of Event
    June 10, 2011
    Report Date
    June 10, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MT, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION UNDERWAY.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PREVENTATIVE MAINTENANCE SCHEDULED IN OUR RECORDS WAS AN INSPECTION OF A COT DROP. THE COT REPORTEDLY DROPPED WITH A PT, HOWEVER, THERE WERE NO ADVERSE CONSEQUENCES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO R-3 AMBULANCE COT STRETCHER, WHEELED INK STRYKER MEDICAL 6082 NA

    Patients

    Seq Age Sex Outcome Treatment
    1