BEUDAMED
    FDA Adverse Event Other Summary report: N

    POISE PADS EXTRA ABSORBENCY

    MDR report key: 586969 · Received April 1, 2005

    Report

    Report Number
    2381757-2005-00003
    Event Type
    Other
    Date Received
    April 1, 2005
    Date of Event
    March 21, 2005
    Report Date
    April 1, 2005
    Manufacturer
    KIMBERLY-CLARK CORP.
    Product Code
    EYQ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    RECEIVED NOTICE IN 2005 ALLEGING THAT A PT HAD RUBBING AND FRICTION RESULTING IN FORMATION OF AN ABSCESS REQUIRING THE DOCTOR TO DRAIN PUS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POISE PADS EXTRA ABSORBENCY INCONTINENCE PAD EYQ KIMBERLY-CLARK CORP. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other