BEUDAMED
    FDA Adverse Event Other Summary report: N

    BARD

    MDR report key: 273212 · Received April 7, 2000

    Report

    Report Number
    273212
    Event Type
    Other
    Date Received
    April 7, 2000
    Date of Event
    February 7, 2000
    Report Date
    March 2, 2000
    Manufacturer
    BARD ACCESS SYSTEMS
    Product Code
    DQO
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    KS, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PHYSICIAN REMOVED CATHETER. TIP BECAME EMBEDDED REQUIRING REMOVAL IN RADIOLOGY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARD GROSHONG CATHETER 8 FR. DQO BARD ACCESS SYSTEMS * 36AJ0082

    Patients

    Seq Age Sex Outcome Treatment
    1 45 YR Other