BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 3083019 · Received April 29, 2013

    Report

    Report Number
    1823260-2013-02612
    Event Type
    Malfunction
    Date Received
    April 29, 2013
    Date of Event
    March 31, 2013
    Report Date
    May 31, 2013
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K031755
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    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 COMPACT PLUS SYSTEM WITHIN 10 MINUTES: 1. 273 MG/DL AND 106 MG/DL 2. 373 MG/DL AND 165 MG/DL SETS OF READINGS WERE TAKEN ON DIFFERENT DAYS. 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
    183492 ACCU-CHEK ® COMPACT TEST DRUM BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 207342

    Patients

    Seq Age Sex Outcome Treatment
    1 073 YR METOPROLOL XL| LOSARTAN POTASSIUM 2X DAILY| LIPITOR| ASPIRIN 1X DAILY| ARANESP| FLUTICASONE PROPIONATE| CITALOPRAM| HYDROCHLOROTHIAZIDE 1X DAILY| VITAMIN C| VITAMIN B6| METFORMIN XL| FOLIC ACID| CENTRUM SILVER| VITAMIN D