BEUDAMED
    FDA Adverse Event Summary report: N

    DR. BROWN'S

    MDR report key: 3927365 · Received July 2, 2014

    Report

    Report Number
    3008138005-2014-00003
    Date Received
    July 2, 2014
    Date of Event
    June 4, 2014
    Report Date
    July 1, 2014
    Manufacturer
    HANDI-CRAFT COMPANY
    Product Code
    HGY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ON (B)(6) 2014 CASE (B)(4) REPORTED THAT SHE HAD EXPERIENCED AN ELECTRIC SHOCK TO HER LEFT NIPPLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    385377 DR. BROWN'S DOUBLE ELECTRIC BREAST PUMP HGY HANDI-CRAFT COMPANY S1006

    Patients

    Seq Age Sex Outcome Treatment
    1 32 YR