BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MICROPORE-SURGICAL TAPE 1X10YDS

    MDR report key: 24647696 · Received March 19, 2026

    Report

    Report Number
    MW5185406
    Event Type
    Injury
    Date Received
    March 19, 2026
    Report Date
    March 12, 2026
    Manufacturer
    3M/ 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

    COMPLAINT: A PERITONEAL DIALYSIS PATIENT REPORTED SHE'S ALLERGIC TO THE PAPER TAPE. IT CAUSES HER SKIN TO BE IRRITATED AND ITCHY. THE REACTION FIRST HAPPENED WHEN SHE FIRST STARTED DIALYSIS. SHE HAS NOT ORDER THEM SINCE THEN BUT NEVER REPORTED THE ALLERGY TO US. THERE WAS PATIENT INVOLVEMENT; HOWEVER, THERE WAS NO HARM OR ADVERSE EVENT 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
    702793 MICROPORE-SURGICAL TAPE 1X10YDS TAPE AND BANDAGE, ADHESIVE KGX 3M/ SOLVENTUM US LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown