BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LOCKING TITANIUM ADAPTER

    MDR report key: 3162966 · Received June 11, 2013

    Report

    Report Number
    1416980-2013-15005
    Event Type
    Malfunction
    Date Received
    June 11, 2013
    Date of Event
    November 6, 2012
    Report Date
    November 7, 2012
    Manufacturer
    KANAE CO.,LTD.
    Product Code
    KDJ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). PER THE CUSTOMER THE SAMPLE WAS NOT AVAILABLE AND THE LOT NUMBER WAS UNKNOWN, THEREFORE NO EVALUATION OR BATCH REVIEW COULD BE PERFORMED.

    Description of Event or Problem · 1

    IT WAS REPORTED TO BAXTER (B)(4) THAT THE PATIENT CONNECTOR WAS NOT CONNECTED WITH THE TITANIUM ADAPTER WELL WHEN THE CUSTOMER CHANGED THE TRANSFER SET. THE CUSTOMER FELT THAT THE JOINT OF EACH CONNECTOR HAS BEEN LOOSE. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION WAS REPORTED. THERE WAS PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    263090 LOCKING TITANIUM ADAPTER SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ KANAE CO.,LTD.

    Patients

    Seq Age Sex Outcome Treatment
    1