BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 1982408 · Received February 9, 2011

    Report

    Report Number
    1823260-2011-00714
    Event Type
    Malfunction
    Date Received
    February 9, 2011
    Date of Event
    January 28, 2011
    Report Date
    February 24, 2011
    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 RESULTS OF 400 MG/DL AND 153 MG/DL WITHIN 10 MINUTES ON THE COMPACT PLUS 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
    1 ACCU-CHEK ® COMPACT TEST DRUM BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 20725747

    Patients

    Seq Age Sex Outcome Treatment
    1 047 YR LASIX| FERROUS SULFATE| XANAX| LORATADINE| NEBULIZER| VITAMIN D| NEURONTIN| "NORVAX"| NOVOLIN NPH| CPAP MACHINE| ASPIRIN| OXYCODONE| 24 HOUR OXYGEN| NOVOLIN R