BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    REACH ACCESS DAILY FLOSSER

    MDR report key: 2932772 · Received January 29, 2013

    Report

    Report Number
    8041101-2013-00012
    Event Type
    Malfunction
    Date Received
    January 29, 2013
    Report Date
    January 4, 2013
    Manufacturer
    JOHNSON & JOHNSON CONSUMER PRODUCTS
    Product Code
    JES
    Removal / Correction Number
    NI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER
    Health Professional
    *

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    39806 REACH ACCESS DAILY FLOSSER DENTAL FLOSS JES JOHNSON & JOHNSON CONSUMER PRODUCTS 8137009658 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown