BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ANIMAS INSULIN INFUSION PUMP

    MDR report key: 1760202 · Received July 12, 2010

    Report

    Report Number
    2531779-2010-00516
    Event Type
    Malfunction
    Date Received
    July 12, 2010
    Date of Event
    April 26, 2010
    Report Date
    June 1, 2010
    Manufacturer
    ANIMAS CORP.
    Product Code
    LZG
    PMA / PMN Number
    K042873
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THERE IS NO ADVERSE EVENT ASSOCIATED WITH THIS COMPLAINT. THE PUMP WAS RETURNED TO ANIMAS FOR EVAL. EVAL REVEALED A DAMAGED FORCE SENSOR ASSEMBLY, AND 'LOSS OF PRIME' WARNINGS WERE CONFIRMED IN THE PUMP HISTORY.

    Description of Event or Problem · 1

    EVAL REVEALED A DAMAGED FORCE SENSOR ASSEMBLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ANIMAS INSULIN INFUSION PUMP INSULIN INFUSION PUMP LZG ANIMAS CORP. ANIMAS 2020 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR