BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    MDR report key: 2110707 · Received June 1, 2011

    Report

    Report Number
    2531779-2011-03853
    Event Type
    Malfunction
    Date Received
    June 1, 2011
    Report Date
    May 3, 2011
    Manufacturer
    ANIMAS CORPORATION
    Product Code
    LZG
    PMA / PMN Number
    K080639
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE PUMP HAS NOT BEEN RETURNED TO ANIMAS FOR EVALUATION. ANIMAS HAS CONDUCTED A REVIEW OF THE DEVICE HISTORY RECORD FOR THIS PUMP AND CONFIRMED THAT IT WAS OPERATING WITHIN REQUIRED SPECIFICATIONS AT THE TIME OF RELEASE. 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.

    Additional Manufacturer Narrative · 1

    (B)(4). DEVICE EVALUATION: THE PUMP HAS BEEN RETURNED AND EVALUATED BY PRODUCT ANALYSIS ON (B)(4) 2011 WITH THE FOLLOWING FINDINGS: A REVIEW OF THE PUMP HISTORY SHOWED ONE REPLACE BATTERY ALARM ASSOCIATED WITH NORMAL BATTERY WEAR. THE PUMP ELECTRICAL DRAWS WERE TESTED AND WERE FOUND TO BE WITHIN THE SPECIFICATIONS.

    Description of Event or Problem · 1

    THIS COMPLAINT IS BEING REPORTED DUE TO THE ALLEGED POWER ISSUE. ACCORDING TO THE PATIENT, THE BATTERY LIFE AVERAGE HAS BEEN GRADUALLY DECREASING OVER THE PAST 2 MONTHS. HER (B)(4) BATTERIES ON AVERAGE LASTED 4 WEEKS. HOWEVER, FOR THE PAST WEEK, HER BATTERY LASTED ONLY 2-3 DAYS. THERE WAS NO REPORTED PATIENT IMPACT ASSOCIATED WITH THIS COMPLAINT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 14 YR