BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 2895145 · Received January 3, 2013

    Report

    Report Number
    1823260-2013-00057
    Event Type
    Malfunction
    Date Received
    January 3, 2013
    Date of Event
    December 15, 2012
    Report Date
    February 18, 2013
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K031755
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, 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 117 MG/DL AND 245 MG/DL WITHIN 10 MINUTES. NO ADVERSE EVENT WAS REPORTED. 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
    3133 ACCU-CHEK ® COMPACT TEST DRUM BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 20734042

    Patients

    Seq Age Sex Outcome Treatment
    1 050 YR POTASSIUM CHLORIDE| METFORMIN| PANTOPRAZOLE| HUMALOG| LANTUS| CPAP SLEEP APNEA MACHINE| AMOXICILLIN| HYDROCODONE/APAP| METOLAZONE| METOPROLOL| LISINOPRIL| FUROSEMIDE