BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HOMECHOICE PRO

    MDR report key: 2181750 · Received July 27, 2011

    Report

    Report Number
    1423500-2011-09856
    Event Type
    Malfunction
    Date Received
    July 27, 2011
    Date of Event
    May 16, 2011
    Report Date
    July 21, 2011
    Manufacturer
    BAXTER HEALTHCARE - LARGO
    Product Code
    FKX
    PMA / PMN Number
    K102936
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE DEVICE WAS RETURNED AND EVALUATED BY THE PRODUCT ANALYSIS LAB (PAL). THE PAL EVALUATED THE DEVICE AND NO FAILURE OR MALFUNCTION WAS IDENTIFIED THAT COULD HAVE CAUSED OR CONTRIBUTED TO THE INCREASED INTRA-PERITONEAL VOLUME (IIPV) FOUND IN THE DEVICE LOGS. THE CAUSE OF THE INCREASED INTRA-PERITONEAL VOLUME (IIPV) WAS DETERMINED TO BE: INSUFFICIENT DRAIN, FALSE EMPTY DETECT AND USE ERROR, INITIAL DRAIN ALARM SETTING INAPPROPRIATELY PROGRAMMED. DEVICE MET SPECIFICATIONS RELATIVE TO IIPV IN THE LOGS.

    Additional Manufacturer Narrative · 1

    (B)(4). THE DEVICE HAS BEEN RECEIVED AT BAXTER FOR EVALUATION. HOWEVER, THE EVALUATION IS NOT COMPLETE AT THIS TIME. A FOLLOW-UP REPORT WILL BE FILED UPON COMPLETION OF THE DEVICE EVALUATION, OR IF ANY ADDITIONAL INFORMATION IS RECEIVED.

    Description of Event or Problem · 1

    DURING A REVIEW OF THE LOGS OF A RETURNED HOMECHOICE (HC) MACHINE, AN INCREASED INTRA-PERITONEAL VOLUME (IIPV) WAS IDENTIFIED DURING DRAIN CYCLE 1. THE PATIENT'S ULTRAFILTRATION (UF) READING WAS 1795 ML, INDICATING THE HOME PATIENT (HP) DRAINED 1795 ML MORE THAN THE LARGEST PRESCRIBED FILL VOLUME OF 2200 ML. THIS MEANT THE TOTAL DRAIN VOLUME WAS APPROXIMATELY 3995 ML, WHICH MEETS THE IIPV CRITERIA. NO PATIENT INJURY OR MEDICAL INTERVENTION WAS REPORTED. PROBABLE CAUSE: INSUFFICIENT DRAIN. FALSE EMPTY DETECT AND USE ERROR. INITIAL DRAIN ALARM SETTING INAPPROPRIATELY PROGRAMMED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HOMECHOICE PRO SYSTEM, PERITONEAL, AUTOMATIC DELIVERY FKX BAXTER HEALTHCARE - LARGO

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR