BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    MDR report key: 3984558 · Received August 6, 2014

    Report

    Report Number
    1823260-2014-05930
    Event Type
    Malfunction
    Date Received
    August 6, 2014
    Date of Event
    July 14, 2014
    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
    MI, US
    Reporter Occupation
    PATIENT
    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: 524 MG/DL AND 199 MG/DL. 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
    459948 ACCU-CHEK ® AVIVA PLUS TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA ASKU

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR Female ACCUPRIL| ARMOUR THYROID| COQ10| COUMADIN| FLEXERIL| FLONASE| FLOVENT| HUMALOG| LANTUS| LASIX| LIPITOR| MAGNESIUM| REQUIP| RESTORIL| SELENIUM| TOPROL| ULTRAM| SELENIUM| FLEXERIL| FLOVENT| LASIX| LIPITOR| LANTUS| HUMALOG| COQ10| REQUIP| FLONASE| ULTRAM| TOPROL| ARMOUR THYROID| ACCUPRIL| COUMADIN| RESTORIL| MAGNESIUM