BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GEM PREMIER 4000

    MDR report key: 2231335 · Received July 25, 2011

    Report

    Report Number
    1217183-2011-00086
    Event Type
    Malfunction
    Date Received
    July 25, 2011
    Date of Event
    May 13, 2011
    Report Date
    July 25, 2011
    Manufacturer
    INSTRUMENTATION LABORATORY, CO.
    Product Code
    CHL
    PMA / PMN Number
    K093623
    Removal / Correction Number
    Z-2803-2011, THROUGH Z-2
    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 PT BLOOD ANALYSIS, LEADING TO ERRONEOUS RESULTS WITH POTENTIALLY SEVERE IMPACT TO PT 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 (B)(4).

    Description of Event or Problem · 1

    CUSTOMER STATED K+ ERROR.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1