BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MICROPORE-SURGICAL TAPE 1X10YDS

    MDR report key: 25244330 · Received May 20, 2026

    Report

    Report Number
    MW5188541
    Event Type
    Injury
    Date Received
    May 20, 2026
    Date of Event
    April 17, 2026
    Report Date
    May 14, 2026
    Manufacturer
    3M COMPANY/SOLVENTUM US LLC
    Product Code
    KGX
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    A PERITONEAL DIALYSIS (PD) PATIENT CONTACTED (B)(6) CUSTOMER SERVICE AND REPORTED THAT THE MICROPORE TAPE CAUSES SKIN IRRITATION AND BREAKOUTS; HOWEVER, THE PATIENT CONTINUES TO USE THE PRODUCT IN LIMITED AMOUNTS. NO ADVERSE EVENT WAS REPORTED. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    31129 MICROPORE-SURGICAL TAPE 1X10YDS TAPE AND BANDAGE, ADHESIVE KGX 3M COMPANY/SOLVENTUM US LLC 16-5301-0

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown