BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MX-PRO AMBULANCE COT

    MDR report key: 2132547 · Received June 10, 2011

    Report

    Report Number
    1831750-2011-05801
    Event Type
    Injury
    Date Received
    June 10, 2011
    Date of Event
    January 9, 2010
    Report Date
    May 3, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION UNDERWAY.

    Description of Event or Problem · 1

    IT WAS REPORTED VIA LEGAL COMPLAINT THAT TWO EMTS WERE ALLEGEDLY INJURED WHILE TRANSPORTING A LARGE PT WHEN THE COT REPORTEDLY FAILED TO LOCK AND COLLAPSED. IT IS ALLEGED THAT THE "KNOB ON THE FAR LEFT SIDE OF THE BLACK RUBBER HANDGRIP INTERFERED WITH THE OPERATION OF THE RED RELEASE AND PREVENTED IT FROM LOCKING BACK IN PLACE." THERE WAS REPORTED PT INVOLVEMENT AND ADVERSE CONSEQUENCES.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 Other