BEUDAMED
    FDA Adverse Event Other Summary report: N

    AIRLIFE MISTY MAX

    MDR report key: 655606 · Received November 16, 2005

    Report

    Report Number
    MW1037204
    Event Type
    Other
    Date Received
    November 16, 2005
    Date of Event
    September 11, 2005
    Report Date
    November 14, 2005
    Manufacturer
    CARDINAL HEALTH CARE CORP.
    Product Code
    CAF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    SUBSTANCE FOUND ON SIDE OF NEBULIZER - TESTED POSITIVE FOR BLOOD. CAME SEALED IN PACKAGING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AIRLIFE MISTY MAX NEBULIZER CAF CARDINAL HEALTH CARE CORP. * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other