BEUDAMED
    FDA Adverse Event Injury Summary report: N

    530G INSULILN PUMP

    MDR report key: 4100788 · Received September 16, 2014

    Report

    Report Number
    2032227-2014-23417
    Event Type
    Injury
    Date Received
    September 16, 2014
    Date of Event
    August 17, 2014
    Report Date
    August 17, 2014
    Manufacturer
    MEDTRONIC MINIMED
    Product Code
    OZO
    PMA / PMN Number
    120010
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    CURRENTLY IT IS UNKNOWN WHETHER OR NOT THE DEVICE MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT AS NO PRODUCT HAS BEEN RETURNED. NO CONCLUSION CAN BE DRAWN AT THIS TIME. WE THEREFORE CONSIDER THIS REPORT COMPLETE TO THE BEST OF OUR KNOWLEDGE. THIS MDR RELATED TO THE PUERTO RICO MANUFACTURING SITE HAS BEEN ASSIGNED A MEDWATCH NUMBER FROM THE MEDTRONIC MINIMED (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE CUSTOMER HAD HIGH BLOOD GLUCOSE LEVELS OF 409 MG/DL. THE CUSTOMER REPORTED A NO DELIVERY ALARM FROM THE INSULIN PUMP THAT WAS RESOLVED BY A COMPLETE INFUSION SET CHANGE. THE CUSTOMER REPORTED THAT THE INFUSION SET AND RESERVOIR HAD AN EXPIRATION DATE OF 2011. EMERGENCY SUPPLIES WERE SHIPPED TO THE CUSTOMER AS A COURTESY. NO ADDITIONAL INFORMATION WAS PROVIDED. PLEASE REFER TO MANUFACTURER'S REPORT NO. 2032227-2014-23416 AS IT REFERS TO THE SAME EVENT BUT OF A DIFFERENT DEVICE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    572238 530G INSULILN PUMP OZO MEDTRONIC MINIMED MMT-751NAP

    Patients

    Seq Age Sex Outcome Treatment
    1 19 YR