BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RENAL - DISPOSABLE

    MDR report key: 1904536 · Received November 22, 2010

    Report

    Report Number
    1423500-2010-06088
    Event Type
    Injury
    Date Received
    November 22, 2010
    Date of Event
    October 1, 2010
    Report Date
    October 29, 2010
    Product Code
    KDJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN
    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 510 (K) NUMBER WILL NOT BE PROVIDED IN THE EMDR AS THE PRODUCT CODE AND LOT NUMBER ARE UNKNOWN. A BATCH REVIEW WILL NOT BE PERFORMED AS THE LOT NUMBER IS UNKNOWN. BAXTER HAS RECEIVED SIMILAR REPORTS FOR THE REPORTED PROBLEM. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED.

    Description of Event or Problem · 1

    THIS IS A SPONTANEOUS REPORT BY A BAXTER EMPLOYED NURSE FROM (B)(6) OF PERITONITIS IN A (B)(6) FEMALE PATIENT. ON (B)(6) 2010, THE PATIENT BEGAN PERITONEAL DIALYSIS(PD). ON (B)(6) 2010, THE PATIENT WAS HOSPITALIZED FOR PERITONITIS. ON THAT SAME DATE, AN EFFLUENT CULTURE WAS DONE AND PD EFFLUENT WAS ANALYZED WITH SAMPLES TAKEN PRIOR TO ANTIBIOTIC THERAPY. AT THE TIME OF REPORTING, THE RESULT OF THE CULTURE WAS UNKNOWN. ON AN UNREPORTED DATE, THE PATIENT BEGAN TREATMENT FOR THE PERITONITIS. THE PATIENT REMAINED HOSPITALIZED AND THE EVENT OF PERITONITIS WAS RESOLVING. PD THERAPY CONTINUED. THE CAUSE OF THE PERITONITIS WAS UNKNOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENAL - DISPOSABLE SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Hospitalization| R DIANEAL PD2 ULTRABAG