BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LTV

    MDR report key: 2072016 · Received April 20, 2011

    Report

    Report Number
    2031702-2011-00083
    Event Type
    Malfunction
    Date Received
    April 20, 2011
    Report Date
    April 20, 2011
    Manufacturer
    CAREFUSION 203, INC.
    Product Code
    CBK
    PMA / PMN Number
    K051767
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    HK
    Reporter Occupation
    NO INFORMATION

    Narratives

    Additional Manufacturer Narrative · 1

    NA

    Description of Event or Problem · 1

    IT WAS REPORTED BY THE FIELD SERVICE CENTER THAT NO FLOW WAS GOING TO THE OUTLET OF THE PT. THE REPORTED PROBLEM OCCURRED DURING A TEST AND THE VENTILATOR WAS NOT CONNECTED TO A PT. IT IS UNK IF THE VENTILATOR AUDIBLY ALARMED WHEN THE REPORTED PROBLEM OCCURRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LTV VENTILATOR, CONTINUOUS / CBK CBK CAREFUSION 203, INC. LTV 1000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA