BEUDAMED
    FDA Adverse Event Other Summary report: N

    ABBOTT

    MDR report key: 252055 · Received November 19, 1999

    Report

    Report Number
    252055
    Event Type
    Other
    Date Received
    November 19, 1999
    Date of Event
    October 29, 1999
    Report Date
    November 19, 1999
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    JHS
    Report Source
    User Facility report
    Reporter Location
    UT, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    AT APPROXIMATELY 1800 ON 10/29/99 THE ABBOTT AXSYM ANALYZER IN THE MAIN LABORATORY RAN OUT OF SOLUTION #3 (MATRIX CELL WASH). THE SENSOR ON THE INSTRUMENT DID NOT ALARM. DURING THIS TIME THE PT WAS TESTED FOR CKBM AND TROPONIN TWICE. THE CARDIOLOGIST RESPONDED WITH A HEARTH CATH PROCEDURE. NOTHING WAS REMARKABLE AND THE PT WAS DISCHARGED TO HIS HOME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT AXSYM JHS ABBOTT LABORATORIES * *

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Other