BEUDAMED
    FDA Adverse Event Injury Summary report: N

    KDJ

    MDR report key: 2180024 · Received July 27, 2011

    Report

    Report Number
    1423500-2011-09732
    Event Type
    Injury
    Date Received
    July 27, 2011
    Date of Event
    July 1, 2011
    Report Date
    July 4, 2011
    Manufacturer
    BAXTER HEALTHCARE
    Product Code
    KDJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NL
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE DEVICES INVOLVED IN THE INCIDENT WERE UNKNOWN. AS THE DATE OF ONSET OF THIS PERITONITIS EPISODE IS UNKNOWN AND PATIENTS DISCARD SUPPLIES AFTER EACH THERAPY, THE SAMPLE WAS NOT REQUESTED. A 510K NUMBER WILL NOT BE PROVIDED IN THE MDR AS THE PRODUCT CODE AND LOT NUMBER ARE UNKNOWN. SINCE THE LOT NUMBER IS UNKNOWN, NO BATCH REVIEW WILL BE PERFORMED. BAXTER HAS RECEIVED SIMILAR REPORTS FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS. THE ROOT CAUSE OF THE REPORTED CONDITION OF PERITONITIS IS UNDETERMINED.

    Description of Event or Problem · 1

    THE FOLLOWING INFORMATION WAS RECEIVED FROM GLOBAL PHARMACOVIGILANCE (GPV): AND IS A SPONTANEOUS REPORT BY A NURSE FROM (B)(6) REPORTING BACTERIAL PERITONITIS IN A PATIENT COINCIDENT WITH PHYSIONEAL 40, UNKNOWN BAG THERAPY. DURING A CALL TO BAXTER CUSTOMER SERVICES, THE NURSE REPORTED THAT THE PATIENT EXPERIENCED PERITONITIS. THE OUTCOME OF THE PERITONITIS AND ACTION TAKEN WITH PHYSIONEAL 40, UNKNOWN BAG WERE NOT REPORTED. THE NURSE BELIEVED THE BACTERIAL PERITONITIS WAS UNRELATED TO PHYSIONEAL 40, UNKNOWN BAG THERAPY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KDJ KDJ BAXTER HEALTHCARE

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Other UNKNOWN BAG| PHYSIONEAL 40