BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AEROCHAMBER

    MDR report key: 172391 · Received June 9, 1998

    Report

    Report Number
    MW1013978
    Event Type
    Injury
    Date Received
    June 9, 1998
    Date of Event
    June 6, 1998
    Report Date
    June 7, 1998
    Manufacturer
    MONAGHAN MEDICAL CORP.
    Product Code
    CCQ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PT USING AEROCHAMBER WITH MDI FOR ASTHMA EXCERBATION WHEN PLASTIC LEAF VALVE DETERMINED MISSING, POSSIBLY ASPIRATED SENDING BRONCHOSCOPY PT EVAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AEROCHAMBER * CCQ MONAGHAN MEDICAL CORP. NA *

    Patients

    Seq Age Sex Outcome Treatment
    1 12 MO Hospitalization