BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SURESTEP ENHANCED

    MDR report key: 369626 · Received December 28, 2001

    Report

    Report Number
    2939301-2001-01714
    Event Type
    Malfunction
    Date Received
    December 28, 2001
    Report Date
    November 15, 2001
    Manufacturer
    LIFESCAN, INC.
    Product Code
    CFR
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    A PATIENT REPORTED EXPERIENCING INACCURATE ERRATIC RESULTS WITH A SSE METER. THE PATIENT'S BLOOD GLUCOSE RESULTS WERE 140, 190 MG/DL. TESTS WERE DONE WITH 10 MINUTES WITH A DIFFERENCE OF 27%. PATIENT DID NOT EXPERIENCE ANY ADVERSE EVENTS. NO FURTHER INFORMATION HAS BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    58751 SURESTEP ENHANCED * CFR LIFESCAN, INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN