BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8022269-2012-00002

    MDR report key: 2484564 · Received March 9, 2012

    Report

    Report Number
    8022269-2012-00002
    Event Type
    Malfunction
    Date Received
    March 9, 2012
    Report Date
    January 21, 2012
    Manufacturer
    JOHNSON & JOHNSON, INC.
    PMA / PMN Number
    K974629
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER
    Health Professional
    N

    Patients

    Seq Age Sex Outcome Treatment
    1 21 YR Female