BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RENAL - DISPOSABLE

    MDR report key: 1904568 · Received November 22, 2010

    Report

    Report Number
    1423500-2010-06092
    Event Type
    Injury
    Date Received
    November 22, 2010
    Date of Event
    January 1, 2010
    Report Date
    October 29, 2010
    Product Code
    KDJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TW
    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 NURSE FROM (B)(6) OF BACTERIAL PERITONITIS WITH (B)(6) IN A FEMALE PATIENT . IN (B)(6) 2009, THE PATIENT BEGAN CONTINUOUS AMBULATORY PERITONEAL DIALYSIS (CAPD). ON AN UNREPORTED DATE IN 2010, THE PATIENT DEVELOPED BACTERIAL PERITONITIS PER (B)(6). ON AN UNREPORTED DATE, DIANEAL PD2 ULTRABAG, AND EXTRANEAL VIAFLEX THERAPIES WERE WITHDRAWN AND THE PATIENT WAS SWITCHED TO HEMODIALYSIS. THE ROOT CAUSE OF THE BACTERIAL PERITONITIS WITH (B)(6) WAS UNKNOWN. IT WAS UNKNOWN WHETHER THE BACTERIAL PERITONITIS WITH (B)(6) RESOLVED.

    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 Required Intervention DIANEAL PD2 ULTRABAG, EXTRANEAL VIAFLEX