BEUDAMED
    FDA Adverse Event Death Summary report: N

    VENELEX OINTMENT

    MDR report key: 9207737 · Received October 17, 2019

    Report

    Report Number
    MW5090455
    Event Type
    Death
    Date Received
    October 17, 2019
    Report Date
    October 16, 2019
    Manufacturer
    TARMAC PRODUCTS, INC.
    Product Code
    FRO
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PATIENT PASSED AWAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    999731 VENELEX OINTMENT DRESSING, WOUND, DRUG FRO TARMAC PRODUCTS, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Death