BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ANIMAS VIBE

    MDR report key: 6776023 · Received August 8, 2017

    Report

    Report Number
    2531779-2017-17703
    Event Type
    Malfunction
    Date Received
    August 8, 2017
    Report Date
    July 18, 2017
    Manufacturer
    ANIMAS CORPORATION
    Product Code
    OYC
    PMA / PMN Number
    P130007
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE PUMP HAS BEEN RETURNED AND EVALUATED BY PRODUCT ANALYSIS ON 07/18/2017 WITH THE FOLLOWING FINDINGS: THE DISPLAY WAS DIM WITH REDDISH TEXT. ANIMAS CORPORATION (B)(4).

    Description of Event or Problem · 1

    THE PUMP WAS RETURNED FOR INVESTIGATION. INVESTIGATION REVEALED THE DISPLAY WAS DIM. THIS REPORT IS MADE BASED ON RESULTS OF INVESTIGATION COMPLETED ON 07/18/2017.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    553899 ANIMAS VIBE INSULIN INFUSION PUMP OYC ANIMAS CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1