BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    MDR report key: 3170703 · Received June 14, 2013

    Report

    Report Number
    1416980-2013-15406
    Event Type
    Injury
    Date Received
    June 14, 2013
    Date of Event
    May 18, 2013
    Report Date
    May 20, 2013
    Manufacturer
    BAXTER HEALTHCARE
    Product Code
    KDJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE CAUSE OF THIS PERITONITIS WAS USE ERROR. PER BAXTER LABELING, USERS ARE INSTRUCTED TO USE ASEPTIC TECHNIQUE WHEN PERFORMING PERITONEAL DIALYSIS THERAPY. A FORMAL REVIEW OF THE LABEL FOR THE PRODUCT FAMILY WILL BE CONDUCTED. IF THERE IS ANY FURTHER RELEVANT INFORMATION FROM THAT REVIEW, A SUPPLEMENTAL MEDWATCH WILL BE FILED.

    Description of Event or Problem · 1

    THIS IS A REPORT OF A HOME PATIENT (HP) WHO DIAGNOSED WITH PERITONITIS. THE CAUSE OF PERITONITIS WAS BREAK IN ASEPTIC TECHNIQUE. THE HP WAS TREATED WITH INJECTION (INJ.) VANCOMYCIN INTRAVENOUS (IV) 1G STAT (CONTINUED FOR 5 DAYS) AND INJ TAZOBACTAM (DESCRIBED AS TAZT)- IV 4.5 G TWICE DAILY (BD).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    271887 SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Required Intervention DIANEAL ULTRABAG