BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ACCU-CHEK D-TRONPLUS

    MDR report key: 1915742 · Received November 29, 2010

    Report

    Report Number
    2183996-2010-02484
    Event Type
    Injury
    Date Received
    November 29, 2010
    Date of Event
    September 22, 2010
    Report Date
    November 19, 2010
    Manufacturer
    ROCHE INSULIN DELIVERY SYSTEMS, INC.
    Product Code
    LZG
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    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. INFO CONTAINED WITHIN THIS REPORT IS ALL THAT IS AVAILABLE AT THIS TIME. IF FURTHER INFO IS OBTAINED, IT WILL BE PROVIDED IN THE SUPPLEMENTAL REPORT.

    Description of Event or Problem · 1

    THE PT REPORTED EXPERIENCING UNEXPLAINABLE ELEVATED BLOOD GLUCOSE OF OVER 350 MG/DL FOR 6-8 WEEKS. HE CHANGED ALL ACCESSORIES AND BOLUSED THROUGH THE INFUSION DEVICE WITH NO SUCCESS. HE INJECTED INSULIN VIA SYRINGE TO LOWER HIS BLOOD GLUCOSE. HE STATED, THE PISTON ROD WORKS "JERKILY" DURING BOLUS AND WHILE PRIMING THE INFUSION TUBING AND AT TIME NO INSULIN DRIPS FROM THE INFUSION TUBING AFTER PRIMING. HE STATED THAT NO E4 (OCCLUSION) ERROR IS DISPLAYED. HE SWITCHED TO HIS BACKUP INFUSION DEVICE AND HIS BLOOD GLUCOSE RETURNED TO NORMAL. HIS NORMAL BLOOD GLUCOSE RANGE IS 80-160 MG/DL. NO FURTHER INFO IS AVAILABLE. THE PT DID NOT REQUIRE TREATMENT FROM A HEALTH CARE PROFESSIONAL OR SECOND PARTY TO ADDRESS THE ISSUE. THE INFUSION DEVICE WAS REPLACED AND REQUESTED TO BE RETURNED FOR EVAL.

    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 Required Intervention INSULIN INFUSION SET| INSULIN