BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2214133-2012-00343

    MDR report key: 2843263 · Received November 22, 2012

    Report

    Report Number
    2214133-2012-00343
    Event Type
    Malfunction
    Date Received
    November 22, 2012
    Report Date
    March 20, 2012
    Manufacturer
    PERSONAL PRODUCTS CO.
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    OTHER
    Health Professional
    *

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown