BEUDAMED
    FDA Adverse Event Summary report: N

    DR. BROWN'S

    MDR report key: 4178116 · Received September 26, 2014

    Report

    Report Number
    3008138005-2014-00005
    Date Received
    September 26, 2014
    Date of Event
    August 28, 2014
    Report Date
    September 26, 2014
    Manufacturer
    HAND-CRAFT COMPANY
    Product Code
    HGX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ON (B)(6), 2014 (B)(6) REPORTED THAT SHE HAD BEEN DIAGNOSED BY A PHYSICIAN WITH MASTITIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    600548 DR. BROWN'S DOUBLE ELECTRIC BREAST PUMP HGX HAND-CRAFT COMPANY S1006

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR