BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® MOBILE TEST STRIPS

    MDR report key: 3254200 · Received July 30, 2013

    Report

    Report Number
    1823260-2013-04586
    Event Type
    Malfunction
    Date Received
    July 30, 2013
    Date of Event
    July 3, 2013
    Report Date
    August 12, 2013
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Additional Manufacturer Narrative · 1

    THE EVENT OCCURRED IN (B)(6). WHILE THIS PRODUCT IS NOT SOLD IN THE UNITED STATES, IT IS LIKE OR SIMILAR TO A PRODUCT MARKETED IN THE UNITED STATES.

    Description of Event or Problem · 1

    REPORTER STATED THAT CUSTOMER RECEIVED THE FOLLOWING RESULTS ON THE MOBILE SYSTEM WITHIN 10 MINUTES: 150 MG/DL AND 71 MG/DL. THE CUSTOMER HAD UNSPECIFIED HYPOGLYCEMIC SYMPTOMS AT THE TIME OF THESE RESULTS. CUSTOMER SELF TREATED WITH SUGAR WATER AND ORANGEJUICE AND BEGAN TO FEEL BETTER. NO ADVERSE EVENT REPORTED. THE MANUFACTURER REQUESTED RETURN OF SUSPECT PRODUCT FOR EVALUATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    355182 ACCU-CHEK ® MOBILE TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 278202

    Patients

    Seq Age Sex Outcome Treatment
    1 027 YR NOVORAPID| LANTUS SOLOSTAR - 1X A DAY