BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIBERTY CYCLER SET, SINGLE CONM. /EXT.DL

    MDR report key: 2980414 · Received February 22, 2013

    Report

    Report Number
    8030665-2013-00111
    Event Type
    Malfunction
    Date Received
    February 22, 2013
    Date of Event
    January 27, 2013
    Report Date
    January 27, 2013
    Manufacturer
    REYNOSA MANUFACTURING
    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 NOT 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 SPEC.

    Description of Event or Problem · 1

    A PERITONEAL DIALYSIS PT HAS REPORTED THAT DIALYSIS SOLUTION WAS LEAKING OUT OF THE CASSETTE AND INTO THE CYCLE. PT OPENED THE CASSETTE DOOR TO REMOVE THE TUBING AND FOUND FLUID LEAKING OUT OF THE CYCLER. PT HAD NO ILL EFFECTS. SAMPLE HAS NOT BEEN RETURNED TO THE MFR; SAMPLE IS NOT AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    77292 LIBERTY CYCLER SET, SINGLE CONM. /EXT.DL LIBERTY DIALYSIS CYCLER TUBING FKX REYNOSA MANUFACTURING 12NR08029

    Patients

    Seq Age Sex Outcome Treatment
    1 LIBERTY DIALYSIS CYCLER