BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MINICAP

    MDR report key: 3052148 · Received April 11, 2013

    Report

    Report Number
    1416980-2013-09013
    Event Type
    Injury
    Date Received
    April 11, 2013
    Report Date
    March 25, 2013
    Manufacturer
    BAXTER HEALTHCARE - CLEVELAND
    Product Code
    KDI
    PMA / PMN Number
    K895631
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). DATE OF EVENT: UNKNOWN DATE IN (B)(6) 2013. AS THE SAMPLE WAS NOT RETURNED, A DEVICE ANALYSIS CANNOT BE COMPLETED. THE CAUSE OF THIS PERITONITIS WAS UNDETERMINED. A BATCH REVIEW OF POTENTIALLY ASSOCIATED LOT NUMBER GD893560 WAS CONDUCTED AND NO ISSUES WERE FOUND RELATED TO THE REPORTED CONDITION DURING THE MANUFACTURE OF THE LOT. (B)(4).

    Description of Event or Problem · 1

    THIS IS A REPORT OF A HOME PATIENT (HP) WHO WAS HOSPITALIZED AND DIAGNOSED WITH PERITONITIS. THE HP WAS TREATED WITH VANCOMYCIN IV AND INTRA-PERITONEALLY (DOSE AND FREQUENCY NOT REPORTED). THE HP WAS RELEASED FROM THE HOSPITAL AND REPORTED TO BE RECOVERING. THIS IS REPORT 2 OF 2 FOR THIS PERITONITIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    156213 MINICAP DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - CLEVELAND

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R DIANEAL 1.5%, 2.5%, 4.25%, CASSETTE AND HOMECHOICE