BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OT VERIO2 METER

    MDR report key: 4911215 · Received July 14, 2015

    Report

    Report Number
    2939301-2015-29120
    Event Type
    Malfunction
    Date Received
    July 14, 2015
    Report Date
    June 29, 2015
    Manufacturer
    LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL
    Product Code
    NBW
    PMA / PMN Number
    K131363
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    ON (B)(6) 2015, THE REPORTER CONTACTED LIFESCAN (B)(4), ALLEGING THAT THE SUBJECT METER READ INACCURATELY LOW WHEN COMPARED TO A ONETOUCH ULTRA METER. THE EXACT METER READINGS WERE NOT AVAILABLE. THIS COMPLAINT IS BEING REPORTED BECAUSE THE METER READINGS MAY NOT HAVE MET LIFESCAN'S CRITERIA FOR ACCURACY AND THE ALLEGED INACCURACY ISSUE WAS NOT RESOLVED WITH TROUBLESHOOTING. THERE WAS NO INDICATION THAT THE PRODUCT CAUSED OR CONTRIBUTED TO AN ADVERSE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    457142 OT VERIO2 METER GLUCOSE MONITORING SYS/KIT NBW LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL 3811629

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR