BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    V200 VENTILATOR

    MDR report key: 3983593 · Received July 9, 2014

    Report

    Report Number
    2031642-2014-00648
    Event Type
    Malfunction
    Date Received
    July 9, 2014
    Report Date
    June 18, 2014
    Manufacturer
    RESPIRONICS CALIFORNIA, INC.
    Product Code
    CBK
    PMA / PMN Number
    K102054
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE INTERNATIONAL CUSTOMER REPORTED THE VENTILATOR WENT VENT INOP DUE TO A FLOW SENSOR FAILURE. VENT INOP, WHEN IN USE, WILL STOP PROVIDING VENTILATORY SUPPORT TO THE PT. THE CUSTOMER REPORTED THE DEVICE WAS NOT IN USE ON A PT THEREFORE, THERE WAS NO PT INVOLVEMENT OR HARM. THE MFR FIELD SERVICE ENGINEER CONFIRMED THE REPORTED PROBLEM. THE MFR'S FIELD SERVICE ENGINEER EVALUATED THE DEVICE AND FOUND THE FLOW SENSOR CABLE WAS DISCONNECTED FROM THE SENSOR BOARD. THE MFR'S FSE REATTACHED THE CABLE TO ADDRESS THE REPORTED PROBLEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    402189 V200 VENTILATOR VENTILATOR, CONTINUOUS CBK RESPIRONICS CALIFORNIA, INC. V200 NA

    Patients

    Seq Age Sex Outcome Treatment
    1