BEUDAMED
    FDA Adverse Event Other Summary report: N

    CELL-DYN 1700

    MDR report key: 247229 · Received October 25, 1999

    Report

    Report Number
    2919069-1999-00019
    Event Type
    Other
    Date Received
    October 25, 1999
    Date of Event
    September 25, 1999
    Report Date
    October 22, 1999
    Manufacturer
    ABBOTT DIAGNOSTICS DIVISION/CELLDYN
    Product Code
    GKZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ON 09/25/1999 AT 06:42 AM, THE ACCOUNT REPORTED A HEMOGLOBIN RESULT OF 18.8 G/DL ON A PT, WHICH WAS QUESTIONED BY THE PHYSICIAN. THE PT WAS RETESTED 11:50 AM, AND A HEMOGLOBIN RESULT OF 8.1 G/DL WAS OBTAINED. THE PT WAS REDRAWN AT 12:15 PM, AND A HEMOGLOBIN RESULT OF 8.7 G/DL WAS OBTAINED. NO REPORT OF INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CELL-DYN 1700 AUTOMATED HEMATOLOGY ANALYZER GKZ ABBOTT DIAGNOSTICS DIVISION/CELLDYN NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 76 YR