BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PROTECTIVE SAFETY IV CATHETER

    MDR report key: 2153220 · Received June 30, 2011

    Report

    Report Number
    MW5021236
    Event Type
    Injury
    Date Received
    June 30, 2011
    Date of Event
    February 20, 2011
    Report Date
    June 30, 2011
    Manufacturer
    SMITHS MEDICAL NORTH AMERICA
    Product Code
    FOZ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    A 20 GA IV CATHETER PLACEMENT, LAC, 1 SITE. ONE ATTEMPT WITH BLOOD DRAW. ULTRASOUND POSITIVE FOR COMPLETE OCCLUSION LEFT BASILIC VEIN. ANTICOAGULANT THERAPY INITIATED AND RESOLUTION WITHOUT APPARENT FURTHER SEQUELAE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PROTECTIVE SAFETY IV CATHETER IV CATHETER FOZ SMITHS MEDICAL NORTH AMERICA * *

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Disability