BEUDAMED
    FDA Adverse Event Other Summary report: N

    KOTEX ULTRATHIN PADS WITH WINGS

    MDR report key: 600813 · Received May 10, 2005

    Report

    Report Number
    2381757-2005-00006
    Event Type
    Other
    Date Received
    May 10, 2005
    Date of Event
    April 12, 2005
    Report Date
    May 10, 2005
    Manufacturer
    KIMBERLY-CLARK CORP.
    Product Code
    HHD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    KIMBERLY CLARK CORPORATION RECEIVED NOTICE IN 2005 ALLEGING THAT THE PATIENT EXPERIENCED HIVES FROM HEAD TO TOE. THE PATIENT ALLEGES THE ALLERGIST CONCLUDED THE HIVES WERE CAUSED BY ULTRATHIN PADS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KOTEX ULTRATHIN PADS WITH WINGS UNSCENTED MENSTRUAL PADS HHD KIMBERLY-CLARK CORP. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other