BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MICROPORE-SURGICAL TAPE 1X10YDS

    MDR report key: 25244324 · Received May 20, 2026

    Report

    Report Number
    MW5188540
    Event Type
    Injury
    Date Received
    May 20, 2026
    Date of Event
    May 1, 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 THEY USED THE TAPE AND SUBSEQUENTLY EXPERIENCED AN ALLERGIC REACTION. THE PATIENT REPORTED ITCHINESS AND REDNESS ON THE AFFECTED AREA OF THE SKIN. 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
    417320 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