BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK SPIRIT

    MDR report key: 1163429 · Received September 10, 2008

    Report

    Report Number
    2183996-2008-01366
    Event Type
    Malfunction
    Date Received
    September 10, 2008
    Date of Event
    August 22, 2008
    Report Date
    August 27, 2008
    Manufacturer
    DISETRONIC MEDICAL SYSTEMS
    Product Code
    LZG
    PMA / PMN Number
    K060876
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    ON (B)(6) 2008 THE PATIENT NOTICED THE DISPLAY OF HIS INFUSION DEVICE WAS BLANK. HE STATED THAT HE INSERTED A NEW BATTERY AND THE DISPLAY REMINDED BLANK. THE PATIENT STATED THAT THE INFUSION DEVICE WAS NOT DROPPED OR EXPOSED TO WATER. HE STATED THAT HE WAS "WANDED" AT THE AIRPORT IN (B)(6) 2008, BUT HE DID NOT RECEIVE ANY ERRORS OR ALARMS. THE PATIENT SWITCHED TO HIS BACKUP INFUSION DEVICE. NO PHYSIOLOGICAL EFFECTS WERE REPORTED. THE PATIENT DID NOT REQUIRE MEDICAL ASSISTANCE FROM A HEALTHCARE PROFESSIONAL OR SECOND PARTY TO ADDRESS THE ISSUE. PRODUCT WAS REPLACED AND REQUESTED TO BE RETURNED FOR EVALUATION.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 37 YR INSULIN INFUSION SET| INSULIN