BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 1970196 · Received January 25, 2011

    Report

    Report Number
    1823260-2011-00380
    Event Type
    Malfunction
    Date Received
    January 25, 2011
    Date of Event
    January 3, 2011
    Report Date
    March 15, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K031755
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CALLER REPORTED COMPACT PLUS BLOOD GLUCOSE RESULTS OF 75 MG/DL, 158 MG/DL, AND 110 MG/DL WITHIN 10 MINUTES. REPORTED NO ADVERSE EVENT. A REQUEST WAS MADE FOR THE RETURN OF THE METER AND STRIPS, REPLACEMENT 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 20728041

    Patients

    Seq Age Sex Outcome Treatment
    1 073 YR FOLIC ACID| SIMVASTATIN| NORVASC| "ALTEST"| METFORMIN 3XDAY| NEURONTIN| SYNTHROID| FISH OIL| OXYCONTIN| ATENOLOL| CALCIUM PILLS