BEUDAMED
    FDA Adverse Event Injury Summary report: N

    IODOSORB POWDER

    MDR report key: 5705423 · Received June 8, 2016

    Report

    Report Number
    8043484-2016-00060
    Event Type
    Injury
    Date Received
    June 8, 2016
    Date of Event
    April 29, 2016
    Report Date
    May 12, 2016
    Manufacturer
    SMITH & NEPHEW MEDICAL LTD.
    Product Code
    KOZ
    PMA / PMN Number
    K870559
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT HAS FOUND TO BE ALLERGIC TO IODOSORB POWDER ON PATCH TESTING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    361602 IODOSORB POWDER BEADS, HYDROPHILIC, FOR WOUND EXUDATE ABSORPTION KOZ SMITH & NEPHEW MEDICAL LTD.

    Patients

    Seq Age Sex Outcome Treatment
    1