BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ARROWGARD HEMODIALYSIS CATHETER

    MDR report key: 8228314 · Received January 7, 2019

    Report

    Report Number
    MW5082937
    Event Type
    Injury
    Date Received
    January 7, 2019
    Date of Event
    January 3, 2019
    Report Date
    January 4, 2019
    Manufacturer
    UNK
    Product Code
    FOZ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    POSSIBLE RETAINED FRAGMENT OF WIRE. ARROW INTERNATIONAL INC., (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    15770 ARROWGARD HEMODIALYSIS CATHETER CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS FOZ UNK 23F18J0007

    Patients

    Seq Age Sex Outcome Treatment
    1 Life Threatening