BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ANIMAS VIBE

    MDR report key: 5150656 · Received October 14, 2015

    Report

    Report Number
    2531779-2015-37153
    Event Type
    Malfunction
    Date Received
    October 14, 2015
    Report Date
    October 7, 2015
    Manufacturer
    ANIMAS CORPORATION
    Product Code
    LZG
    PMA / PMN Number
    P130007
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PATIENT

    Narratives

    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. (B)(6).

    Additional Manufacturer Narrative · 1

    DEVICE EVALUATION: THE PUMP HAS BEEN RETURNED AND EVALUATED BY PRODUCT ANALYSIS ON 11/12/2015 WITH THE FOLLOWING FINDINGS. ON INVESTIGATION, THE ALLEGED BUTTON TACTILE ISSUE WAS NOT DUPLICATED. THE PUMP POWERED UP TO THE DISPLAY SCREEN WITH AUDITORY AND VIBRATORY FEATURES. THE KEYPAD COVER WAS INTACT AND ALL THE BUTTONS RESPONDED PROPERLY. REMOVAL OF THE KEYPAD COVER DID NOT FIND ANY ANOMALIES WITH THE BUTTON CONTACTS. UNRELATED TO THE COMPLAINT, VERTICAL BLACK LINES WERE OBSERVED RUNNING THROUGH THE TEXT IN THE DISPLAY SCREEN.

    Description of Event or Problem · 1

    ON (B)(6) 2015, THE REPORTER CONTACTED ANIMAS, ALLEGING A BUTTON/KEYPAD (TACTILE CHANGES/UNRESPONSIVE) ISSUE WITH THE 'OK' BUTTON. NO ADDITIONAL DETAIL WAS PROVIDED. NO ADDITIONAL DETAIL WAS PROVIDED. 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
    679111 ANIMAS VIBE INSULIN INFUSION PUMP LZG ANIMAS CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1