BEUDAMED
    FDA Adverse Event Other Summary report: N

    ABBOTT

    MDR report key: 155667 · Received February 13, 1998

    Report

    Report Number
    155667
    Event Type
    Other
    Date Received
    February 13, 1998
    Date of Event
    July 16, 1997
    Report Date
    July 24, 1997
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    JHS
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    AR, US
    Reporter Occupation
    MEDICAL TECHNOLOGIST

    Narratives

    Description of Event or Problem · 1

    CKMB REPORTED 20.3. PT REC'D RETROVACE AS A RESULT OF THE INCORRECT RESULTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT IMX CKMB REACTION MATRIX CELL JHS ABBOTT LABORATORIES IMX 27202M200

    Patients

    Seq Age Sex Outcome Treatment
    1 36 YR Other