BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    MDR report key: 2920677 · Received January 17, 2013

    Report

    Report Number
    1823260-2013-00332
    Event Type
    Malfunction
    Date Received
    January 17, 2013
    Date of Event
    January 3, 2013
    Report Date
    July 28, 2025
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K101299
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 1

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

    Description of Event or Problem · 1

    CUSTOMER REPORTEDLY RECEIVED THE FOLLOWING RESULTS ON THE AVIVA SYSTEM WITHIN 10 MINUTES: 111 MG/DL AND 66 MG/DL. NO ACTIONS TAKEN BASED ON DEVICE RESULTS. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT DEVICE AND STRIPS, AND REPLACEMENT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    26363 ACCU-CHEK ® AVIVA PLUS TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 491006

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Male ASPIRIN| CITALOPRAM| CLONIDINE| FERROUS SULFATE| FOLIC ACID| HUMALOG| ISOSORB MONO| LEVEMIR| LEVOTHYROXINE| LOSARTAN| NITROSTAT| PACE MAKER| PLAVIX| POLYETHYLENE GLYCOL| QUINAPRIL| RANEXA| RANITIDINE| TAMSULOSIN| POLYETHYLENE GLYCOL| LOSARTAN| ASPIRIN| LEVOTHYROXINE| LEVEMIR| HUMALOG| PLAVIX| CLONIDINE| CITALOPRAM| PACE MAKER| FERROUS SULFATE| TAMSULOSIN| RANITIDINE| QUINAPRIL| ISOSORB MONO| NITROSTAT| FOLIC ACID| RANEXA