BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LTV

    MDR report key: 2001765 · Received January 7, 2011

    Report

    Report Number
    2031702-2011-00253
    Event Type
    Malfunction
    Date Received
    January 7, 2011
    Report Date
    January 7, 2011
    Manufacturer
    CAREFUSION 203, INC.
    Product Code
    CBK
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NA

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE VENTILATOR'S TURBINE STOPPED OPERATING - NO AIR WAS BEING BLOWN OUT OF VENTILATOR. THE VENTILATOR ALARMED FOR LOW MINUTE VOLUME. THE VENTILATOR WAS NOT CONNECTED TO A PT, THIS HAPPENED DURING TESTING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LTV VENTILATOR, CONTINUOUS / CBK CBK CAREFUSION 203, INC. LTV 950 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NI