BEUDAMED
    FDA Adverse Event Summary report: N

    LTV

    MDR report key: 1963288 · Received January 11, 2011

    Report

    Report Number
    2031702-2011-00256
    Date Received
    January 11, 2011
    Report Date
    January 11, 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
    TX, US
    Reporter Occupation
    RESPIRATORY THERAPIST

    Narratives

    Additional Manufacturer Narrative · 1

    NA

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE VENTILATOR HAD MULTIPLE ALARM CONDITIONS AND SHUT DOWN WHILE CONNECTED TO A PATIENT. THE PATIENT WAS PLACED ON A BACK-UP VENTILATOR. NO PATIENT HARM REPORTED.

    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