BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MINICAP

    MDR report key: 3250957 · Received July 29, 2013

    Report

    Report Number
    1416980-2013-19957
    Event Type
    Injury
    Date Received
    July 29, 2013
    Date of Event
    January 22, 2013
    Report Date
    July 2, 2013
    Manufacturer
    BAXTER HEALTHCARE - CLEVELAND
    Product Code
    KDI
    PMA / PMN Number
    K895631
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS WAS PERFORMED FOR POTENTIALLY ASSOCIATED LOT NUMBER GD293297 WITH NO ISSUES NOTED DURING THE MANUFACTURING PROCESS THAT WAS RELATED TO THE REPORTED ISSUE. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. THIS IS THE SAME PATIENT AS (B)(4).

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A PERITONEAL DIALYSIS (PD) PATIENT EXPERIENCED PERITONITIS WHILE IN THE HOSPITAL FOR SEVERE BACK PAIN. THE NURSE REPORTED THE CAUSE OF THE PERITONITIS WAS DIARRHEA WHICH HAD CROSSED OVER THE PERITONEAL MEMBRANE. TREATMENT FOR THE PERITONITIS INCLUDED ZYBOX, ORAL (DOSE AND FREQUENCY NOT REPORTED). ON AN UNREPORTED DATE, THE PATIENT WAS DISCHARGED FROM THE HOSPITAL. AT THE TIME OF THE INITIAL REPORT, THE PATIENT WAS NOT RECOVERED FROM THE PERITONITIS EVENT. THIS IS REPORT 3 OF 3 INVOLVED IN THIS PERITONITIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    352584 MINICAP DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - CLEVELAND

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Required Intervention HOMECHOICE AUTOMATED PD SET WITH CASSETTE| MINICAP TRANSFER SET| DIANEAL PD4, 2.5% AMBUFLEX, LOW CALCIUM| DIANEAL PD4, 4.25% AMBUFLEX, LOW CALCIUM