BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TRANSPORE-PLASTIC TRANS. TAPE 1"X10YDS/ 16

    MDR report key: 25014819 · Received April 27, 2026

    Report

    Report Number
    MW5187322
    Event Type
    Injury
    Date Received
    April 27, 2026
    Date of Event
    April 7, 2026
    Report Date
    April 21, 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 TO REPORT THAT THE 16-1527-7, TRANSPORE-PLASTIC TRANS. TAPE IRRITATES HER SKIN. SHE STATED THAT SHE GETS RED AND SOME BLEEDING. SHE STATED THAT THIS HAPPENS WITH ALL TYPES OF TAPE IN HER PRESCRIPTION ORDER. 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
    1055048 TRANSPORE-PLASTIC TRANS. TAPE 1"X10YDS/ 16 TAPE AND BANDAGE, ADHESIVE KGX SOLVENTUM US LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown