BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GEM PREMIER 4000

    MDR report key: 2231333 · Received July 25, 2011

    Report

    Report Number
    1217183-2011-00088
    Event Type
    Malfunction
    Date Received
    July 25, 2011
    Date of Event
    June 3, 2011
    Report Date
    July 25, 2011
    Manufacturer
    INSTRUMENTATION LABORATORY CO.
    Product Code
    CIG
    PMA / PMN Number
    K093623
    Removal / Correction Number
    Z-2803-2011
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THERE IS A KNOWN ISSUE ON THE GEM PREMIER 4000 SYSTEM OF FALSELY LOWERED K+ RESULTS (POTENTIAL NEGATIVE BIAS OF 0.6 TO 2.0 MMOL/L) THAT CAN OCCUR DURING CARTRIDGE LIFE ON PATIENT BLOOD ANALYSIS, LEADING TO ERRONEOUS RESULTS WITH POTENTIALLY SEVERE IMPACT TO PATIENT TREATMENT. RECALL; A RECALL HAS BEEN INITIATED TO NOTIFY THE FIELD REGARDING THE ISSUE WITH K+ REPORTING ON THE GEM PREMIER 4000. THIS RECALL ACTION WAS SUBMITTED AND WILL BE TRACKED THROUGH THE LOCAL (B)(6) FDA DISTRICT OFFICE (B)(6). RECALL X-2803-2011 THROUGH Z-2806-2011.

    Description of Event or Problem · 1

    CUSTOMER STATED THAT THERE WAS TOO MUCH FLUCTUATION IN POTASSIUM STUDY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GEM PREMIER 4000 BLOOD GAS / CO-OXIMETRY ANALYZER CIG INSTRUMENTATION LABORATORY CO. 4000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1