BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RENAL - DISPOSABLE

    MDR report key: 1863911 · Received October 11, 2010

    Report

    Report Number
    1423500-2010-04284
    Event Type
    Injury
    Date Received
    October 11, 2010
    Date of Event
    September 1, 2010
    Report Date
    September 17, 2010
    Product Code
    KDJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    RP
    Reporter Occupation
    OTHER

    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.

    Description of Event or Problem · 1

    THIS IS A SPONTANEOUS REPORT BY A CONSUMER FROM THE (B)(6) OF FEVER, BREAK IN ASEPTIC TECHNIQUE AND PERITONITIS IN A PATIENT COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. ON AN UNKNOWN DATE, A BREAK IN ASEPTIC TECHNIQUE DESCRIBED AS "DID NOT WEAR A MASK" AND A FEVER OCCURRED. ON (B)(6) 2010, THE PATIENT WAS DIAGNOSED WITH PERITONITIS MANIFESTED BY 1WEEK ABDOMINAL PAIN, CLOUDY EFFLUENT, LOW GRADE FEVER AND ABDOMINAL TENDERNESS. THE CAUSE OF THE PERITONITIS WAS A BREAK IN ASEPTIC TECHNIQUE. THE PATIENT WAS HOSPITALIZED ON (B)(6) 2010 FOR THE PERITONITIS. ON AN UNKNOWN DATE, THE REMEDIAL MEDICATION OF CIPROBAY (500MG, BID) WAS STARTED. IT WAS NOT REPORTED WHETHER THE PATIENT WAS RETRAINED IN ASEPTIC TECHNIQUE. IT WAS UNKNOWN IF PD THERAPY WAS ONGOING. IT WAS UNKNOWN IF THE PERITONITIS RESOLVED. THE REPORTER BELIEVED THAT THE PERITONITIS WAS NOT RELATED TO THE PD THERAPY, BUT WAS DUE TO THE BREAK IN ASEPTIC TECHNIQUE. A CAUSALITY STATEMENT WAS NOT REPORTED FOR THE BREAK IN ASEPTIC TECHNIQUE OR THE FEVER.

    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 47 YR Hospitalization| R DIANEAL PD2,CATAPRES, CALCIUM CARBONATE AND EPOGEN