BEUDAMED
    FDA Adverse Event Injury Summary report: N

    16-1535-0, MICROPORE-PAPER TAPE 1X10YDS W/DISPENSER

    MDR report key: 24278785 · Received February 5, 2026

    Report

    Report Number
    MW5183455
    Event Type
    Injury
    Date Received
    February 5, 2026
    Date of Event
    January 22, 2026
    Report Date
    February 3, 2026
    Manufacturer
    3M COMPANY/SOLVENTUM
    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 CUSTOMER SERVICE TO REPORT THAT SHE IS ALLERGIC TO THE MICROPORE-PAPER TAPE 1X10YDS W/DISPENSER. PATIENT DOES NOT HAVE ANYTHING TO RETURN. SHE DISCARDED THE TAPE. 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
    336142 16-1535-0, MICROPORE-PAPER TAPE 1X10YDS W/DISPENSER TAPE AND BANDAGE, ADHESIVE KGX 3M COMPANY/SOLVENTUM

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown