BEUDAMED
    FDA Adverse Event Other Summary report: N

    ELASTOPLAST TAPE

    MDR report key: 30334 · Received February 20, 1996

    Report

    Report Number
    MW1008379
    Event Type
    Other
    Date Received
    February 20, 1996
    Date of Event
    January 17, 1996
    Report Date
    February 9, 1996
    Manufacturer
    BEIERSDORF, INC.
    Product Code
    KGX
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    TAPE WAS USED TO SECURE PLASTIC TUBING USED FOR LABOR EPIDURAL ON PT'S BACK. PT EXPERIENCED SIGNIFICANT CONTACT DERMATITIS WHERE TAPE WAS IN CONTACT WITH SKIN WHICH BLISTERED. RESOLVED AFTER 7-10 DAYS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ELASTOPLAST TAPE TAPE KGX BEIERSDORF, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 32 YR Other LABOR EPIDURAL, LOCAL ANESTHETIC(S), STADOL