BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INOMAX DS (DELIVERY SYSTEM)

    MDR report key: 1880378 · Received October 15, 2010

    Report

    Report Number
    3004531588-2010-00102
    Event Type
    Malfunction
    Date Received
    October 15, 2010
    Date of Event
    July 21, 2010
    Report Date
    October 15, 2010
    Manufacturer
    INO THERAPEUTICS LLC/IKARIA
    Product Code
    MRN
    PMA / PMN Number
    K061901
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ON (B)(6) 2010, A RESPIRATORY THERAPIST REPORTED NITRIC OXIDE (NO) SENSOR FAILURE ON INOMAX DS # (B)(4). EVAL SUMMARY: ON INVESTIGATION, WE WERE UNABLE TO DUPLICATE THE REPORTED CONDITION WITH THIS DEVICE. HOWEVER, ON EXAMINATION OF THE DEVICE SERVICE LOG, FLUCTUATING MONITORED NITRIC OXIDE (NO) VALUES WERE RECORDED. SINCE FLUCTUATING MONITORED (NO) VALUES HAVE BEEN OBSERVED IN THE SERVICE LOGS OF OTHER DEVICES AND HAVE BEEN LINKED TO FRETTING CORROSION OF AN INTERNAL RIBBON CABLE, THE CABLE WAS REPLACED. THE FRETTING CORROSION CAN LEAD TO INTERMITTENT HIGH RESISTANCE CONNECTION AT THE CABLE'S CONNECTOR, LEADING TO FLUCTUATING MONITORED (NO) VALUES. IT IS IMPORTANT TO NOTE THAT THE MONITORED (NO) VALUES WOULD BE FLUCTUATING IN THIS CASE AND NOT THE ACTUAL (NO) DELIVERED.

    Description of Event or Problem · 1

    ON (B)(6) 2010, A RESPIRATORY THERAPIST REPORTED NITRIC OXIDE (NO) SENSOR FAILURE ON INOMAX DS # (B)(4). THE DEVICE WAS NOT ON A PT AND NO ADVERSE EVENT WAS REPORTED BY THE RESPIRATORY THERAPIST. THE DEVICE WAS REMOVED FROM SERVICE BY THE CUSTOMER AND RETURNED TO THE COMPANY FOR INVESTIGATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INOMAX DS (DELIVERY SYSTEM) APPARATUS, NITRIC OXIDE DELIVERY MRN INO THERAPEUTICS LLC/IKARIA 10003

    Patients

    Seq Age Sex Outcome Treatment
    1