BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIBERTY CYCLER SET, DUAL PATIENT CONN/EXT.DL

    MDR report key: 2970099 · Received February 15, 2013

    Report

    Report Number
    8030665-2013-00097
    Event Type
    Malfunction
    Date Received
    February 15, 2013
    Date of Event
    January 19, 2013
    Report Date
    January 19, 2013
    Manufacturer
    ERIKA DE REYNOSA, S.A. DE C.V.
    Product Code
    FKX
    PMA / PMN Number
    K043363
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE WAS NOT RETURNED TO THE MFR FOR PHYSICAL EVAL AND THE FAILURE MODE CANNOT BE CONFIRMED. HOWEVER, AN INVESTIGATION OF THE DEVICE MFG RECORDS WAS CONDUCTED BY THE MFR. THERE WERE NO DEVIATIONS OR NONCONFORMANCES DURING THE MFG PROCESS. IN ADDITION, THE BATCH RECORD REVIEW CONFIRMED THE LABELING, MATERIAL, AND PROCESS CONTROLS WERE WITHIN SPECIFICATION.

    Description of Event or Problem · 1

    A PERITONEAL DIALYSIS PATIENT HAS REPORTED THAT DIALYSIS SOLUTION WAS LEAKING OUT OF CASSETTE AND INTO THE CYCLER. THE LEAK WAS NOTICED WHEN THE PATIENT WAS STILL CONNECTED TO THE CYCLER AND THE DOOR WAS CLOSED. PT HAD NO ILL EFFECTS. SAMPLE WAS DISCARDED BY THE PATIENT; SAMPLE IS NOT AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    66918 LIBERTY CYCLER SET, DUAL PATIENT CONN/EXT.DL LIBERTY DIALYSIS CYCLER TUBING FKX ERIKA DE REYNOSA, S.A. DE C.V. 12LR08070

    Patients

    Seq Age Sex Outcome Treatment
    1 LIBERTY DIALYSIS CYCLER