BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEILMED SINUS RINSE

    MDR report key: 11392203 · Received February 26, 2021

    Report

    Report Number
    MW5099687
    Event Type
    Injury
    Date Received
    February 26, 2021
    Report Date
    February 25, 2021
    Manufacturer
    NEILMED PHARMACEUTICALS, INC.
    Product Code
    KCJ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    LACK OF EFFICACY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    280978 NEILMED SINUS RINSE APPLICATOR, ENT KCJ NEILMED PHARMACEUTICALS, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Other