BEUDAMED
    FDA Adverse Event Summary report: N

    DR. BROWN'S

    MDR report key: 3651319 · Received February 19, 2014

    Report

    Report Number
    3008138005-2014-00001
    Date Received
    February 19, 2014
    Date of Event
    January 23, 2014
    Report Date
    February 19, 2014
    Manufacturer
    HANDI-CRAFT COMPANY
    Product Code
    HGY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

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

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    103832 DR. BROWN'S DOUBLE ELECTRIC BREAST PUMP HGY HANDI-CRAFT COMPANY S1006 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK