BEUDAMED
    FDA Adverse Event Other Summary report: N

    "AROSHY" CATHETER

    MDR report key: 32671 · Received May 3, 1996

    Report

    Report Number
    MW4001165
    Event Type
    Other
    Date Received
    May 3, 1996
    Date of Event
    March 20, 1996
    Report Date
    April 12, 1996
    Manufacturer
    BARD ACCESS SYSTEM
    Product Code
    DQO
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    TPN LEAKED THROUGH CATHETER CAUSING SWELLING OF THE ANTERIOR CHEST WALL IN RECOVERY. DEFECTIVE CATHETER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 "AROSHY" CATHETER CATHETER DQO BARD ACCESS SYSTEM

    Patients

    Seq Age Sex Outcome Treatment
    1 44 YR Other