BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 1982409 · Received February 9, 2011

    Report

    Report Number
    1823260-2011-00713
    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 THE FOLLOWING RESULTS ON THE COMPACT PLUS SYSTEM WITHIN 10 MINUTES: 331 MG/DL, 146 MG/DL, HI (GREATER THEN 600 MG/DL), AND 139 MG/DL. 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 OXYCODONE| LASIX| NEURONTIN| ASPIRIN| XANAX| CPAP MACHINE| NOVOLIN R| NOVOLIN "NPH"| 24 HOUR OXYGEN| NEBULIZER| "NORVAX"| LORATADINE| VITAMIN D| FERROUS SULFATE