BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® MOBILE TEST STRIPS

    MDR report key: 2801649 · Received October 23, 2012

    Report

    Report Number
    1823260-2012-05335
    Event Type
    Malfunction
    Date Received
    October 23, 2012
    Date of Event
    October 2, 2012
    Report Date
    January 7, 2013
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    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

    CALLER REPORTED MOBILE SYSTEM BLOOD GLUCOSE RESULTS OF 18.7 MMOL/L AND 7.9 MMOL/L WITHIN 10 MINUTES. NO ADVERSE EVENT WAS REPORTED. 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 278163

    Patients

    Seq Age Sex Outcome Treatment
    1 049 YR LIPITOR 40 MG, 1/DAY| AMLODIPINE 5 MG 2/DAY| CHLORTALIDONE 50 MG, ONE A DAY| RIMIPRIL 5 MG BD 2X/DAY| GLUCOPHAGE, METFORMIN 1000 MG, 2/DAY