BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    MDR report key: 3820228 · Received May 20, 2014

    Report

    Report Number
    1823260-2014-03549
    Event Type
    Malfunction
    Date Received
    May 20, 2014
    Date of Event
    April 22, 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
    NY, 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 RESULTS OF 312 MG/DL AND 144 MG/DL WITHIN 10 MINUTES ON THE AVIVA SYSTEM. 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
    299457 ACCU-CHEK ® AVIVA PLUS TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 492214

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Female BUMEX| DIGOXIN| INDERAL| LANTUS| LEXAPRO| LOPRESSOR| NEBULIZER| NOVOLOG FLEXPEN| POTASSIUM| QUINAPRIL| XANAX| XARELTO| POTASSIUM| NOVOLOG FLEXPEN| XARELTO| LANTUS| DIGOXIN| QUINAPRIL| NEBULIZER| INDERAL| LEXAPRO| XANAX| LOPRESSOR| BUMEX