BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2050012-2011-00280

    MDR report key: 1974421 · Received January 31, 2011

    Report

    Report Number
    2050012-2011-00280
    Event Type
    Malfunction
    Date Received
    January 31, 2011
    Date of Event
    January 5, 2011
    Report Date
    January 5, 2011
    Manufacturer
    BECKMAN COULTER, INC.
    PMA / PMN Number
    K042291
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER
    Health Professional
    *

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown