BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    MDR report key: 3142146 · Received June 3, 2013

    Report

    Report Number
    1416980-2013-14042
    Event Type
    Malfunction
    Date Received
    June 3, 2013
    Date of Event
    May 10, 2013
    Report Date
    May 11, 2013
    Manufacturer
    BAXTER HEALTHCARE - MOUNTAIN HOME
    Product Code
    FKX
    PMA / PMN Number
    K923065
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THIS REPORT IS FOR A SYSTEM ERROR 2240, WHERE THE HOME PATIENT PRESSED GO BEFORE CONNECTING. PER THE BAXTER HOMECHOICE OPERATOR'S MANUAL, PATIENTS ARE TO CONNECT TO THE SETUP PRIOR TO PRESSING GO. A REVIEW OF THE LABEL FOR THE PRODUCT FAMILY WILL BE CONDUCTED. IF THERE IS ANY FURTHER RELEVANT INFORMATION, A SUPPLEMENTAL MEDWATCH WILL BE FILED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT WHILE PERFORMING PERITONEAL DIALYSIS, A HOME PATIENT (HP) RECEIVED A SYSTEM ERROR 2240 (AIR IN SET) ON A HOMECHOICE (HC) MACHINE DURING DWELL TWO OF THREE. THE HP HAD PRESSED GO BEFORE CONNECTING TO THE HC. THE TECHNICAL SERVICE REPRESENTATIVE (TSR) EXPLAINED THAT THE HP NEEDS TO BE CONNECTED TO THE HC AT THE BEGINNING OF THERAPY. THE TSR ASSISTED THE HP IN CLEARING THE ALARM AND ADVISED THE HP TO START OVER WITH NEW SUPPLIES. THERE WAS PATIENT INVOLVEMENT, BUT NO PATIENT INJURY OR MEDICAL INTERVENTION WAS INDICATED IN ASSOCIATION WITH THIS REPORT. NO ADDITIONAL INFORMATION IS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    244712 HOMECHOICE AUTOMATED PD SET WITH CASSETTE SYSTEM, PERITONEAL, AUTOMATIC DELIVERY FKX BAXTER HEALTHCARE - MOUNTAIN HOME

    Patients

    Seq Age Sex Outcome Treatment
    1 86 YR HOMECHOICE