BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    MDR report key: 4141374 · Received October 3, 2014

    Report

    Report Number
    2531779-2014-28343
    Event Type
    Malfunction
    Date Received
    October 3, 2014
    Report Date
    September 23, 2014
    Manufacturer
    ANIMAS CORPORATION
    Product Code
    LZG
    PMA / PMN Number
    K080639
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE EVALUATION: THE DEVICE HAS BEEN RETURNED AND EVALUATED BY PRODUCT ANALYSIS ON 11/07/2014 WITH THE FOLLOWING FINDINGS: THE BLACK BOX RECORDED A LOSS OF PRIME WARNING ON (B)(6) 2014 DUE TO A LOW, NON-ZERO, FORCE SENSOR READING. THE PUMP WAS EXERCISED FOR 24 HOURS AT 1 UNIT/HOUR RATE WITH NO LOSS OF PRIME WARNINGS OR OTHER ALARMS NOTED. THE FORCE SENSOR WAS FOUND TO BE PROPERLY CALIBRATED. THE ALLEGED ISSUE COULD NOT BE DUPLICATED DURING INVESTIGATION BUT COULD BE FOUND IN THE DEVICE'S HISTORY.

    Additional Manufacturer Narrative · 1

    THE PUMP HAS NOT BEEN RETURNED TO ANIMAS FOR EVALUATION. IF THE DEVICE IS RETURNED, AN EVALUATION SHALL BE COMPLETED AND A SUPPLEMENTAL REPORT WILL BE FILED. NO CONCLUSIONS CAN BE MADE AT THIS TIME.

    Description of Event or Problem · 1

    ON (B)(6) 2014, THE REPORTER CONTACTED ANIMAS, ALLEGING THAT THERE WERE REPEATED LOSS OF PRIME WARNINGS WITH DIFFERENT CARTRIDGES. THIS COMPLAINT IS BEING REPORTED BECAUSE THE REPORTED ISSUE WAS NOT RESOLVED WITH TROUBLESHOOTING. THERE WAS NO INDICATION THAT THE PRODUCT CAUSED OR CONTRIBUTED TO AN ADVERSE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    620509 ONETOUCHPING GLUCOSEMGMTSYSTEM INSULIN INFUSION PUMP LZG ANIMAS CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 13 YR