BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 1821898 · Received August 31, 2010

    Report

    Report Number
    1823260-2010-05172
    Event Type
    Malfunction
    Date Received
    August 31, 2010
    Date of Event
    August 12, 2010
    Report Date
    August 31, 2010
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K031755
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, 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

    REPORTER ALLEGED OBTAINING THE RESULTS OF 280 MG/DL AND 85 MG/DL BACK TO BACK WITHIN 10 MINUTES ON THE COMPACT PLUS SYSTEM. NO ACTIONS WERE REPORTED TAKEN OR TREATMENT RECEIVED. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE AFFECTED PRODUCT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK ® COMPACT TEST DRUM BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 20725045

    Patients

    Seq Age Sex Outcome Treatment
    1 055 YR PROVIGIL| LIPITOR| "CENTURA"| CYMBALTA| FLORINEF| METHADONE| LANTUS| REQUIP| B 12 INJECTION| ARAVA| LORAZEPAM| LYRICA| ZANAFLEX| FOLIC ACID| PREDNISONE