BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    I-STAT EC8+ CARTRIDGE

    MDR report key: 20389327 · Received October 7, 2024

    Report

    Report Number
    2245578-2024-00186
    Event Type
    Malfunction
    Date Received
    October 7, 2024
    Date of Event
    August 31, 2024
    Report Date
    November 22, 2024
    Manufacturer
    ABBOTT POINT OF CARE
    Product Code
    CHL
    PMA / PMN Number
    K940918
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    APOC INCIDENT: # (B)(4). THE INVESTIGATION WAS COMPLETED ON 21-NOV-2024. A REVIEW OF THE DEVICE HISTORY RECORD (DHR) CONFIRMED THE CARTRIDGE LOT MET FINISHED GOODS (FG) RELEASE CRITERIA. RETAINED CARTRIDGE TESTING MET THE ACCEPTANCE CRITERIA OUTLINED IN APPENDIX 1 OF Q04.01.003 REV AN, PRODUCT COMPLAINT LEVEL 2 AND LEVEL 3 INVESTIGATION PROCEDURE. NO DEFICIENCY HAS BEEN IDENTIFIED FOR EC8+ CARTRIDGE LOT K24082 AND CG8+ CARTRIDGE LOT W24205.

    Additional Manufacturer Narrative · 0

    APOC INCIDENT # (B)(4). APOC LABELING WILL BE EVALUATED DURING THE INVESTIGATION AS PERTAINING TO THE EVENT.

    Description of Event or Problem · 0

    NA.

    Description of Event or Problem · 0

    ON 01-OCT-2024, ABBOTT POINT OF CARE WAS CONTACTED BY A CUSTOMER REGARDING I-STAT EC8+ CARTRIDGES THAT YIELDED SUSPECTED DISCREPANT POTASSIUM RESULTS ON A 50 YEAR OLD MALE PATIENT WITH PNEUMONIA, AND A TRAUMA PATIENT.. THERE WAS NO ADDITIONAL PATIENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT. RETURN PRODUCT IS NOT AVAILABLE FOR INVESTIGATION. METHOD: I-STAT, DATE: (B)(6) 2024, COLLECTED: 20:26; 20:27, TESTED: 7.39, PH: A, SAMPLE: HEMOLYZED. METHOD: I-STAT, DATE: (B)(6) 2024, COLLECTED: 20:26; 20:35, TESTED: 7.33, PH: A. METHOD: I-STAT, DATE: (B)(6) 2024, COLLECTED: 20:50; 20:52, TESTED: 7.144, PH: B. METHOD: GEM 5000, DATE: (B)(6) 2024, COLLECTED: 20:50; 20:58, TESTED: 7.31, PH: B. AT THIS TIME THERE IS NO REASON TO SUSPECT A MALFUNCTION EXISTS. THE REPORTING DECISION WAS BASED ON THE LIMITED INFORMATION AVAILABLE THAT SUGGESTS THE PRODUCT WAS NOT PERFORMING WITHIN THE VARIABILITY OF THE ASSAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2546628 I-STAT EC8+ CARTRIDGE EC8+ CARTRIDGE CHL ABBOTT POINT OF CARE NA K24082

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Male