BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ANIMAS INSULIN INFUSION PUMP

    MDR report key: 1132433 · Received August 22, 2008

    Report

    Report Number
    2531779-2008-00511
    Event Type
    Malfunction
    Date Received
    August 22, 2008
    Date of Event
    July 21, 2008
    Report Date
    July 21, 2008
    Manufacturer
    ANIMAS CORORATION
    Product Code
    LZG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE PUMP WAS RETURNED TO ANIMAS FOR EVALUATION. EVALUATION REVEALED AN INTERMITTENT LOSS OF CONTACT BETWEEN THE BATTERY CAP AND THE PUMP CASE.

    Description of Event or Problem · 1

    THE PATIENT'S MOTHER REPORTED THAT UPON USE OF A BATTERY CAP SHIPPED IN 2008, THE PUMP WAS RESETTING ITSELF WITHOUT INTERVENTION, BUT WHEN THE OLD BATTERY CAP WAS USED, THE PUMP FUNCTIONED NORMALLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ANIMAS INSULIN INFUSION PUMP INSULIN INFUSION PUMP LZG ANIMAS CORORATION IR-1250

    Patients

    Seq Age Sex Outcome Treatment
    1