BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RENAL - DISPOSABLE

    MDR report key: 1871429 · Received October 15, 2010

    Report

    Report Number
    1423500-2010-04442
    Event Type
    Injury
    Date Received
    October 15, 2010
    Date of Event
    September 1, 2010
    Report Date
    September 23, 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 PATIENT DISCARDED SUPPLIES AFTER EACH THERAPY, THE SAMPLE WAS NOT REQUESTED. A 510K NUMBER WILL NOT BE PROVIDED IN THE EMDR AS THE PRODUCT CODE AND LOT NUMBER ARE UNKNOWN. BAXTER HAS RECEIVED SIMILAR REPORTS FOR THE REPORTED PROBLEM.

    Description of Event or Problem · 1

    IN (B)(6)2010, THE PATIENT STARTED PERITONEAL DIALYSIS (PD) TREATMENT. ON (B)(6)2010, THE PATIENT WAS DIAGNOSED WITH PERITONITIS. THE CAUSE OF THE PERITONITIS WAS UNKNOWN. ON THE SAME DAY, A PERITONEAL EFFLUENT ANALYSIS AND CULTURE WERE PERFORMED. THE ANALYSIS AND CULTURE RESULTS WERE NOT REPORTED. ON (B)(6)2010, THE PATIENT BEGAN REMEDIAL THERAPY WITH FORTUM (1GM, DAILY, INTRAPERITONEAL (IP) AND REFLIN (500MG, DAILY, IP). PD THERAPY WAS ONGOING. IT WAS UNKNOWN WHETHER THE PERITONITIS RESOLVED. NO CONCOMITANT MEDICATIONS WERE REPORTED. THE NURSE BELIEVED THAT THE EVENT OF PERITONITIS WAS NOT RELATED TO PD THERAPY.

    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 58 YR Required Intervention DIANEAL PD2 ULTRABAG