BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8041101-2012-00207

    MDR report key: 2791953 · Received October 16, 2012

    Report

    Report Number
    8041101-2012-00207
    Event Type
    Malfunction
    Date Received
    October 16, 2012
    Report Date
    February 6, 2012
    Manufacturer
    JOHNSON & JOHNSON CONSUMER PRODUCTS
    Removal / Correction Number
    NI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER
    Health Professional
    *

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown