BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    D-TRONPLUS

    MDR report key: 1030566 · Received April 15, 2008

    Report

    Report Number
    2183996-2008-00549
    Event Type
    Malfunction
    Date Received
    April 15, 2008
    Date of Event
    April 11, 2008
    Report Date
    April 11, 2008
    Manufacturer
    DISETRONIC MEDICAL SYSTEMS
    Product Code
    LZG
    PMA / PMN Number
    K043000
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IN 2008, THE PT REPORTED THAT AN ERROR MESSAGE WAS DISPLAYED ON THE SCREEN OF HIS INFUSION DEVICE, BUT HE WAS UNABLE TO DETERMINE WHICH ERROR BECAUSE THE SCREEN IS DAMAGED. HE STATED THE SCREEN HAD BEEN DAMAGED FOR "A WHILE." HE INSTALLED A NEW BATTERY AND THE INFUSION DEVICE CONTINUED TO BEEP. NO PHYSIOLOGICAL EFFECTS WERE REPORTED. THE PT DID NOT REQUIRE MEDICAL ASSISTANCE FROM A HEALTHCARE PROFESSIONAL OR SECOND PARTY TO ADDRESS THE ISSUE. PRODUCT WAS REQUESTED TO BE RETURNED FOR EVAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 D-TRONPLUS INSULIN INFUSION PUMP LZG DISETRONIC MEDICAL SYSTEMS NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 INSULIN| INSULIN INFUSION SET