BEUDAMED
    FDA Adverse Event Summary report: N

    BRONCOTRON-I

    MDR report key: 1029963 · Received April 11, 2008

    Report

    Report Number
    1029963
    Date Received
    April 11, 2008
    Date of Event
    February 23, 2008
    Report Date
    March 31, 2008
    Manufacturer
    PERCUSSIONAIRE CORPORATION
    Product Code
    CBK
    Report Source
    User Facility report
    Reporter Location
    UT, US

    Narratives

    Description of Event or Problem · 1

    TRANSPORT VENTILATOR WAS CONNECTED TO PATIENT AND FUNCTIONING IN THE HF MODE AT 580-600 BPM WITH MEAN AIRWAY PRESSURE SET AT 10. WORKING PRESSURE WAS BETWEEN 30-38 PSI. WHILE TRANSPORTING, MEAN AIRWAY PRESSURE (MAP) BEGAN TO RISE. PEEP VALVE WAS ADJUSTED BUT PRESSURE CONTINUED TO RISE. PEEP VALVE WAS REMOVED AND PRESSURE CONTINUED TO RISE REACHING 20. VENTILATOR WAS REMOVED FROM PATIENT AND BABY HAND-BAGGED WHILE VENTILATOR PHASITRON WAS CHECKED FOR PROBLEMS. UNABLE TO FIND PROBLEM. UNABLE TO ACHIEVE SATS IN 90'S, EVEN WITH HAND BAGGING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BRONCOTRON-I VENTILATOR CBK PERCUSSIONAIRE CORPORATION BRONCHOTRON-I N/A

    Patients

    Seq Age Sex Outcome Treatment
    1 1 DA