BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 2962161 · Received February 14, 2013

    Report

    Report Number
    0001831750-2013-01174
    Event Type
    Malfunction
    Date Received
    February 14, 2013
    Date of Event
    January 20, 2013
    Report Date
    January 22, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    IT WAS ALSO FOUND DURING THE INVESTIGATION THAT THE X-FRAME BASE WAS ALSO LEANING DUE TO THE DAMAGE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY REPAIR WORK ORDER THAT THE CUSTOMER ALLEGED THAT THE FRAME TRIGGER WAS STICKING.

    Description of Event or Problem · 1

    IT WAS REPORTED BY REPAIR WORK ORDER THAT THE CUSTOMER ALLEGED THAT THE FRAME TRIGGER WAS STICKING AND THE X-FRAME BASE WAS LEANING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    64636 MX-PRO R-3 AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1