BEUDAMED
    FDA Adverse Event Other Summary report: N

    KOTEX ULTRATHIN PADS WITH WINGS

    MDR report key: 584869 · Received March 24, 2005

    Report

    Report Number
    2381757-2005-00002
    Event Type
    Other
    Date Received
    March 24, 2005
    Date of Event
    February 25, 2005
    Report Date
    March 24, 2005
    Manufacturer
    KIMBERLY CLARK CORPORATION
    Product Code
    HEB
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    KIMBERLY CLARK CORPORATION RECEIVED NOTICE IN 2005 ALLEGING THAT A PTIENT HAD IRRITATION WITH A RED BUMPY RASH THAT TURNED INTO AN ABCESS REQUIRING A SURGICAL PROCEDURE TO LANCE THE ABCESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KOTEX ULTRATHIN PADS WITH WINGS UNSCENTED MENSTRUAL PAD HEB KIMBERLY CLARK CORPORATION NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other