BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MICROPORE SURGICAL TAPE

    MDR report key: 24412944 · Received February 23, 2026

    Report

    Report Number
    MW5184176
    Event Type
    Injury
    Date Received
    February 23, 2026
    Date of Event
    December 17, 2025
    Report Date
    February 17, 2026
    Manufacturer
    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 PATIENT REPORTED THAT THE PAPER TAPE USED TO SECURE THE TUBING CAUSES ITCHING IN THE AREA WHERE IT IS APPLIED. 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
    472918 MICROPORE SURGICAL TAPE TAPE AND BANDAGE, ADHESIVE KGX SOLVENTUM US LLC. 108229728

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown