BEUDAMED
    FDA Adverse Event Other Summary report: N

    KY HIS AND HERS

    MDR report key: 4352572 · Received December 12, 2014

    Report

    Report Number
    MW5039676
    Event Type
    Other
    Date Received
    December 12, 2014
    Date of Event
    December 11, 2014
    Report Date
    December 12, 2014
    Product Code
    NUC
    Report Source
    Voluntary report
    Reporter Location
    HI, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAVE BOUGHT A KY YOURS AND HIS PRODUCT AND IT CAUSED INFLAMING IRRITATION IN PRIVATE AREAS AND MY OTHER HALF TO HAVE RAW SKIN IRRITATION AND IN HIS PRIVATE AREAS AS WELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    808296 KY HIS AND HERS KY HIS AND HERS NUC

    Patients

    Seq Age Sex Outcome Treatment
    1 6 MO Other