BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MICROPORE-PAPER TAPE 1X10YDS W/DISPENSER

    MDR report key: 25244316 · Received May 20, 2026

    Report

    Report Number
    MW5188539
    Event Type
    Injury
    Date Received
    May 20, 2026
    Date of Event
    April 15, 2026
    Report Date
    May 14, 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 (PD) PATIENT CONTACTED (B)(6) CUSTOMER SERVICE AND REPORTED THAT THE PATIENT HAS A STATED ALLERGY TO TAPE AND IS UNABLE TO USE SILK TAPE BUT USES PAPER TAPE. THE PATIENT REPORTED THAT USE OF PAPER TAPE RESULTS IN BUMPS BUT DOES NOT CAUSE A BREAKOUT AS WOULD OCCUR WITH USE OF SILK TAPE. THE PATIENT STATED THAT SHE WILL CONTINUE USING PAPER TAPE AS IT IS THE ONLY AVAILABLE OPTION. 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
    417319 MICROPORE-PAPER TAPE 1X10YDS W/DISPENSER TAPE AND BANDAGE, ADHESIVE KGX SOLVENTUM US LLC 16-1535-0

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown