BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® AVIVA TEST STRIPS

    MDR report key: 1954633 · Received January 10, 2011

    Report

    Report Number
    1823260-2011-00143
    Event Type
    Malfunction
    Date Received
    January 10, 2011
    Date of Event
    December 31, 2010
    Report Date
    January 27, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K043474
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND

    Narratives

    Description of Event or Problem · 1

    CUSTOMER REPORTEDLY RECEIVED THE FOLLOWING RESULTS ON THE AVIVA SYSTEM WITHIN 10 MINUTES: 468 MG/DL AND 132 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 302980

    Patients

    Seq Age Sex Outcome Treatment
    1 052 YR TOPAMAX| TRAZODONE| ABILIFY| ZOLOFT| LAMOTRIGINE| "SUVILA"| NEURONTIN| ZOCOR| LASIX| CONTINUOUS OXYGEN| REGLAN| NEXIUM| DETROL LA AT BEDTIME| ZANTAC| "NITRO"| LYRICA