BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® AVIVA TEST STRIPS

    MDR report key: 2170779 · Received July 21, 2011

    Report

    Report Number
    1823260-2011-03884
    Event Type
    Malfunction
    Date Received
    July 21, 2011
    Date of Event
    July 10, 2011
    Report Date
    September 19, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K043474
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    IT WAS UNKNOWN IF THE INITIAL REPORTER SENT REPORT TO THE FDA.

    Description of Event or Problem · 1

    REPORTER ALLEGED THE CUSTOMER RECEIVED THE RESULTS OF 388 MG/DL, 46 MG/DL AND 50 MG/DL BACK TO BACK WITHIN 10 MINUTES ON THE AVIVA SYSTEM. NO ACTIONS WERE REPORTED TAKEN OR TREATMENT RECEIVED. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE AFFECTED PRODUCT.

    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 303194

    Patients

    Seq Age Sex Outcome Treatment
    1 081 YR ASPIRIN (DAILY)| "GLIPI" (TWICE DAILY)| PROTONIX (DAILY)| MULTIVITAMIN (DAILY)| LEVOTHYROXINE (DAILY)| FLOMAX (DAILY)| IRON (TWICE DAILY)| ZOCOR (DAILY)| SEROQUEL (3 TIMES DAILY)| ALDACTONE (TWICE DAILY)| TORSEMIDE (DAIILY)| COREG (TWICE DAILY)| VENTOLIN INHALER (EVERY 8 HOURS)