BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 2972284 · Received February 21, 2013

    Report

    Report Number
    1823260-2013-01108
    Event Type
    Malfunction
    Date Received
    February 21, 2013
    Date of Event
    January 30, 2013
    Report Date
    March 1, 2013
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Additional Manufacturer Narrative · 1

    THE EVENT OCCURRED IN (B)(6). THIS MEDWATCH IS FOR THE COMPACT PLUS SYSTEM 2. (B)(6).

    Description of Event or Problem · 1

    REPORTER STATED THAT PATIENT RECEIVED THE FOLLOWING RESULTS, WITH TWO DIFFERENT METERS, WITHIN 1-2 MINUTES: HI (RESULT OVER 33.3 MMOL/L), 7.0 MMOL/L (COMPACT PLUS SYSTEM 1), 7.0 MMOL/L (COMPACT PLUS SYSTEM 2); 22.0 MMOL/L OR 23.6 MMOL/L (UNABLE TO DETERMINE WHICH ACTUAL RESULT WAS RECEIVED), 7.0 MMOL/L (COMPACT PLUS SYSTEM 1), 7.0 MMOL/L (COMPACT PLUS SYSTEM 2.) SETS OF READINGS WERE TAKEN AT DIFFERENT TIMES. NO ACTIONS TAKEN BASED ON DEVICE RESULTS. NO ADVERSE EVENT REPORTED. THE MANUFACTURER REQUESTED RETURN OF SUSPECT PRODUCT FOR EVALUATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    76939 ACCU-CHEK ® COMPACT TEST DRUM BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA ASKU

    Patients

    Seq Age Sex Outcome Treatment
    1 069 YR