BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2008K2 HEMODIALYSIS MACHINE

    MDR report key: 4102195 · Received September 17, 2014

    Report

    Report Number
    2937457-2014-02728
    Event Type
    Malfunction
    Date Received
    September 17, 2014
    Date of Event
    August 8, 2014
    Report Date
    August 22, 2014
    Manufacturer
    FRESENIUS MEDICAL CARE NORTH AMERICA, CONCORD MANUFACTURING
    Product Code
    KDI
    PMA / PMN Number
    K994267
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION FINDINGS TO DATE INDICATED THE REPORTED MALFUNCTION OCCURRED DURING RECIRCULATION AND PRIME (MACHINE SET-UP), AND NOT DURING DIALYSIS MODE. THE USER VISUALLY OBSERVED THE SALINE BAG FILLING WITH DIALYSATE DURING CIRCULATION. THERE HAVE BEEN NO ADVERSE EVENTS ASSOCIATED WITH THE REPORTED ISSUE. THE REPORT IS BEING INVESTIGATED BY THE MANUFACTURER VIA A CAPA. THE INVESTIGATION IS PENDING A SUPPLEMENTAL MDR WILL BE FILED AT THE COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    A USER FACILITY REPORTED A SALINE BAG BACK FILLED DURING RECIRCULATION MODE. A PATIENT WAS NOT CONNECTED TO THE MACHINE AT THE TIME OF THE INCIDENT. FACILITY REPORTED THAT THEY REPLACED THE AIR SEPARATOR AND VALVE 43. ADDITIONAL ATTEMPTS TO THE CUSTOMER HAVE BEEN MADE WITH NO ADDITIONAL INFORMATION PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    575991 2008K2 HEMODIALYSIS MACHINE KDI FRESENIUS MEDICAL CARE NORTH AMERICA, CONCORD MANUFACTURING

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN SALINE (DISCARDED-NOT USED)