BEUDAMED
    FDA Adverse Event Death Summary report: N

    AEROSET ANALYZER

    MDR report key: 296528 · Received September 14, 2000

    Report

    Report Number
    1628664-2000-00056
    Event Type
    Death
    Date Received
    September 14, 2000
    Date of Event
    August 3, 2000
    Report Date
    September 13, 2000
    Manufacturer
    ABBOTT MFG, INC.
    Product Code
    JJE
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    A POTASSIUM RESULT OF 2.9MMOL/L WAS REPORTED OUT OF THE LAB. THE PT WAS TREATED WITH POTASSIUM INFUSION DUE TO THIS LOW RESULT. THIS TREATMENT CAUSED THE PT TO GO INTO CARDIAC ARREST AND DIE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AEROSET ANALYZER CLINICAL CHEMISTRY ANALYZER JJE ABBOTT MFG, INC. NI NI

    Patients

    Seq Age Sex Outcome Treatment
    1 75 YR Death ICT MODULE LIST NUMBER 9D28.