BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PLEURX DRAINAGE CATHETER

    MDR report key: 8777093 · Received July 9, 2019

    Report

    Report Number
    MW5088001
    Event Type
    Injury
    Date Received
    July 9, 2019
    Date of Event
    July 7, 2019
    Report Date
    July 7, 2019
    Manufacturer
    CAREFUSION 2200, INC.
    Product Code
    PNG
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PERITONITIS RELATED TO PLEURX DRAINAGE CATHETER FOR ASCITES RELATED TO ALCOHOLIC CIRRHOSIS. FDA SAFETY REPORT ID# (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    568090 PLEURX DRAINAGE CATHETER PERITONEAL, DRAINAGE CATHETER FOR REFRACTORY ASCITES, LONG-TERM INDWELLING PNG CAREFUSION 2200, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Hospitalization| L