BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® AVIVA TEST STRIPS

    MDR report key: 1911808 · Received December 1, 2010

    Report

    Report Number
    1823260-2010-07069
    Event Type
    Malfunction
    Date Received
    December 1, 2010
    Date of Event
    November 23, 2010
    Report Date
    February 25, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Additional Manufacturer Narrative · 1

    THE EVENT OCCURRED IN (B)(6).

    Description of Event or Problem · 1

    CUSTOMER REPORTEDLY RECEIVED THE FOLLOWING RESULTS ON THE AVIVA SYSTEM WITHIN 10 MINUTES: 3.4 MMOL/L, 3.1 MMOL/L. AND 6.7 MMOL/L. NO ACTIONS TAKEN BASED ON DEVICE RESULTS. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT DEVICE.

    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 202807

    Patients

    Seq Age Sex Outcome Treatment
    1 080 YR LIPITOR ONCE DAILY| GABAPENTIN ONCE DAILY| VERAPAMIL TWICE DAILY| VITAMIN B12 ONCE A DAY| "EUROFER" ONCE DAILY| PAROXETINE| RABEPRAZOLE TWICE DAILY| METFORMIN TWICE DAILY| DOMPERIDONE 4 TIMES A DAY| RALOXIFENE ONCE DAILY