BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK D-TRONPLUS

    MDR report key: 1982132 · Received January 14, 2011

    Report

    Report Number
    2183996-2011-00022
    Event Type
    Malfunction
    Date Received
    January 14, 2011
    Date of Event
    January 3, 2011
    Report Date
    January 6, 2011
    Manufacturer
    ROCHE INSULIN DELIVERY SYSTEMS, INC.
    Product Code
    LZG
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS INCIDENT OCCURRED OUTSIDE THE UNITED STATES. INFORMATION CONTAINED WITHIN THIS REPORT IS ALL THAT IS AVAILABLE AT THIS TIME. IF FURTHER INFORMATION IS OBTAINED, IT WILL BE PROVIDED IN THE SUPPLEMENTAL REPORT.

    Description of Event or Problem · 1

    THE PATIENT REPORTED EXPERIENCING INSULIN IN THE CARTRIDGE COMPARTMENT OF THE INFUSION DEVICE SINCE (B)(6) 2011 AND ELEVATED BLOOD GLUCOSE OF 192 MG/DL. THE PATIENT CHANGED THE ACCESSORIES AND BOLUSED THROUGH THE INFUSION DEVICE AND VIA PEN TO LOWER BLOOD GLUCOSE. ON (B)(6) 2011, E1 (EMPTY CARTRIDGE) ERROR WAS DISPLAYED. THE PATIENT CHANGED THE INSULIN CARTRIDGE AND ADAPTER AND NO INSULIN DRIPPED FROM THE INFUSION TUBING. THERE WAS AGAIN INSULIN IN THE CARTRIDGE COMPARTMENT. THE PATIENT REPORTED NO A4 (CARTRIDGE/ADAPTER) ALERT OF E4 (OCCLUSION) ERROR WAS DISPLAYED. NO FURTHER INFORMATION IS AVAILABLE. THE PATIENT DID NOT REQUIRE TREATMENT FROM A HEALTH CARE PROFESSIONAL OR SECOND PARTY TO ADDRESS THE ISSUE. THE INFUSION DEVICE AND ADAPTER WERE REPLACED AND REQUESTED TO BE RETURNED FOR EVALUATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK D-TRONPLUS INSULIN INFUSION PUMP LZG ROCHE INSULIN DELIVERY SYSTEMS, INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR INSULIN| INSLUIN INFUSION SET