BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP

    MDR report key: 3231092 · Received July 12, 2013

    Report

    Report Number
    9615050-2013-02027
    Event Type
    Malfunction
    Date Received
    July 12, 2013
    Manufacturer
    HOSPIRA COSTA RICA LTD.
    Product Code
    FRN
    PMA / PMN Number
    K982159
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER CONTACT INDICATED THAT THE DEVICE WAS DISCARDED. INVESTIGATION IS NOT COMPLETE. THIS REPORT REPRESENTS ALL THE INFO KNOWN BY THE REPORTER UPON QUERY BY HOSPIRA PERSONNEL.

    Description of Event or Problem · 1

    THE CUSTOMER CONTACT REPORTED THE CLAVE SECONDARY PORT REMAINED IN THE DEPRESSED POSITION. ON AN UNSPECIFIED DATE, THE PRIMARY TUBING SET WAS BEING USED TO DELIVER AN UNSPECIFIED MEDICATION, AT AN UNSPECIFIED RATE, VIA A PLUM PUMP. AFTER AN UNSPECIFIED LENGTH OF TIME, THE CUSTOMER CONTACT REPORTED THAT THE MALE ADAPTER OF A NEEDLELESS VALVE CONNECTOR CONNECTED TO AN UNSPECIFIED SECONDARY TUBING SET WAS CONNECTED TO THE CLAVE SECONDARY PORT ON THE CASSETTE OF THE PRIMARY TUBING SET FOR A PIGGYBACK DELIVERY OF AN UNSPECIFIED CHEMOTHERAPEUTIC AGENT. AFTER AN UNSPECIFIED LENGTH OF TIME AFTER THE PIGGYBACK DELIVERY WAS STARTED, IT WAS REPORTED THAT THE PUMP ALARMED FOR AIR IN LINE. THE CUSTOMER CONTACT REPORTED THAT THE NURSE BACKPRIMED THE PUMP TO CLEAR THE ALARM. IT WAS REPORTED THAT THE NURSE COULD NOT CLEAR THE AIR IN LINE ALARM AND DISCONNECTED THE NEEDLELESS VALVE CONNECTOR FROM THE CLAVE SECONDARY PORT. AT THIS TIME, IT WAS NOTED THAT THE SILICONE SLEEVE OF THE CLAVE SECONDARY PORT REMAINED IN THE DEPRESSED POSITION. THE PRIMARY TUBING SET WAS REPLACED AND THE THERAPY WAS RESUMED. THERE WERE NO REPORTED ADVERSE PATIENT EFFECTS AND NO REPORTED DELAY IN THERAPY CRITICAL TO THIS PT. NO MEDICAL INTERVENTIONS WERE REQUIRED. THOUGH REQUESTED, NO ADDITIONAL INFO WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    324783 PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP 80FRN FRN HOSPIRA COSTA RICA LTD. NA 261125H

    Patients

    Seq Age Sex Outcome Treatment
    1 SPIROS CONNECTOR: LIST # UNK, MFR ICU MEDICAL| UNSPECIFIED SECONDARY TUBING SET: LIST # UNK,| LOT # UNK