BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK MOBILE TEST STRIPS

    MDR report key: 2143133 · Received June 28, 2011

    Report

    Report Number
    1823260-2011-03493
    Event Type
    Malfunction
    Date Received
    June 28, 2011
    Date of Event
    June 8, 2011
    Report Date
    June 29, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Additional Manufacturer Narrative · 1

    THE EVENT OCCURRED IN (B)(6).

    Description of Event or Problem · 1

    CALLER REPORTED SYMPTOMS OF HYPOGLYCEMIA ON (B)(6) 2011, MOBILE SYSTEM BLOOD GLUCOSE RESULTS OF 6.1 MMOL/L, 11.6 MMOL/L, 3.0 MMOL/L, AND 4.8 MMOL/L WITHIN 10 MINUTES. REPORTED NO ADVERSE EVENT. ALSO REPORTED SYMPTOMS OF HYPOGLYCEMIA ON (B)(6) 2011, MOBILE SYSTEM BLOOD GLUCOSE RESULTS OF 10 MMOL/L, 6.5 MMOL/L, 3.3 MMOL/L, AND 3.1 MMOL/L WITHIN 10 MINUTES. REPORTED NO ADVERSE EVENT. A REQUEST WAS MADE FOR THE RETURN OF THE METER AND STRIPS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK MOBILE TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 278033

    Patients

    Seq Age Sex Outcome Treatment
    1 013 YR