BEUDAMED
    FDA Adverse Event Other Summary report: N

    KOTEX LIGHTDAYS DEODORANT PANTILINERS

    MDR report key: 578989 · Received March 7, 2005

    Report

    Report Number
    2381757-2005-00001
    Event Type
    Other
    Date Received
    March 7, 2005
    Date of Event
    February 16, 2005
    Report Date
    March 7, 2005
    Manufacturer
    KIMBERLY CLARK CORPORATION
    Product Code
    HHD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    KIMBERLY CLARK CORPORATION RECEIVED NOTICE IN 2005 ALLEGING THAT A A PATIENT HAD IRRITATION WITH ITCHING, SORENESS AND SWELLING. ACCORDING TO THE COMPLAINT, THE PATIENT VISITED A DOCTOR WHO ALLEGED THAT IRRITATION WAS CAUSED FROM THE PADS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KOTEX LIGHTDAYS DEODORANT PANTILINERS DEODORANT PANTILINER HHD KIMBERLY CLARK CORPORATION NA UK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other