BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FASTTAKE

    MDR report key: 388819 · Received April 12, 2002

    Report

    Report Number
    2939301-2002-05168
    Event Type
    Malfunction
    Date Received
    April 12, 2002
    Report Date
    April 3, 2002
    Manufacturer
    LIFESCAN, INC.
    Product Code
    CFR
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    A PATIENT REPORTED EXPERIENCING INACCURATE ERRATIC RESULTS WITH A FT, METER. THE PATIENT'S BLOOD GLUCOSE RESULTS WERE 140, 200 MG/DL. TESTS WERE DONE WITHIN LESS THAN 10 MINUTES WITH A DIFFERENCE OF 31%. PATIENT DID NOT EXPEIRENCE ANY ADVERSE EVENTS. NO FURTHER INFORMATION HAS BEEN REPORTED. NOTE: CUSTOMER USING EXPIRED CONTROL SOLUTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FASTTAKE BLOOD GLUCOSE MONITORING KIT/SYSTEM CFR LIFESCAN, INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR