BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 3091980 · Received May 3, 2013

    Report

    Report Number
    1823260-2013-02724
    Event Type
    Malfunction
    Date Received
    May 3, 2013
    Date of Event
    April 7, 2013
    Report Date
    June 13, 2013
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K031755
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, 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

    CALLER REPORTED COMPACT PLUS SYSTEM BLOOD GLUCOSE RESULTS OF 146 MG/DL, 261 MG/DL, AND 309 MG/DL WITHIN 10 MINUTES. NO ADVERSE EVENT WAS REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE STRIPS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    193908 ACCU-CHEK ® COMPACT TEST DRUM BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 20731445

    Patients

    Seq Age Sex Outcome Treatment
    1 069 YR ASPIRIN 1X A DAY| GLIMEPIRIDE 2XDAY| LIPITOR 1XDAY| PLAVIX 1X A DAY| LOSARTAN 1XDAY| CARPETILOL| MEFORMIN 2XDAY| "TARP/LEVO"