BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® AVIVA TEST STRIPS

    MDR report key: 1933086 · Received December 20, 2010

    Report

    Report Number
    1823260-2010-07555
    Event Type
    Malfunction
    Date Received
    December 20, 2010
    Date of Event
    December 14, 2010
    Report Date
    January 10, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K043474
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CUSTOMER REPORTEDLY RECEIVED THE FOLLOWING RESULTS ON THE AVIVA SYSTEM WITHIN 10 MINUTES: 593 MG/DL AND 139 MG/DL. NO ACTIONS TAKEN BASED ON DEVICE RESULTS. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT DEVICE AND REPLACEMENT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK ® AVIVA TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 302927

    Patients

    Seq Age Sex Outcome Treatment
    1 061 YR PLAVIX| CILOSTAZOL| GLYBURIDE| NEBULIZER| NOVOLOG| CYMBALTA| LEVEMIR| PRILEPTAL| SYNTHROID| TEMAZEPAM| XANAX| DARVOCET| LORCET| OXYGEN| LASIX| BENICAR| ENALAPRIL| PRANDIN| TWO INHALERS - TYPE UNKNOWN| LORATADINE| C-PAP