BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ONE TOUCH ULTRA

    MDR report key: 652690 · Received December 8, 2005

    Report

    Report Number
    2939301-2005-05574
    Event Type
    Malfunction
    Date Received
    December 8, 2005
    Report Date
    December 2, 2005
    Manufacturer
    LIFESCAN, INC.
    Product Code
    NBW
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    THE PATIENT REPORTED BLOOD GLUCOSE RESULTS OF "293, 116, 156, 161, 125, AND 121 MG/DL" WITH A LIFESCAN METER, PERFORMED WITHIN 11-20 MINUTES OF EACH OTHER. THE METER, TEST STRIPS, AND CONTROL SOLUTION WERE REPLACED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ONE TOUCH ULTRA GLUCOSE MONITORING SYS/KIT NBW LIFESCAN, INC. NA 2523980

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN