Events

Field Safety Notices about Smart Flex Vascular Stent System

According to Turkey Drugs and Medical Devices Agency (Titck), this field safety notices involved a device in Turkey that was produced by Cordis a Cardinal Health Company.

What is this?

Field safety notices are communications sent out by medical device manufacturers or their representatives in relation to actions that they may be taking in relation to their product that is on the market. These are mainly for health workers, but also for users. They can include recalls and alerts.

Learn more about the data here
  • Type of Event
    Field Safety Notice
  • Event ID
    2017/234 & Cordis20170216
  • Date
    2017-02-22
  • Event Country
    Turkey
  • Event Source
    TDMDAT
  • Event Source URL
    https://web.archive.org/web/20171014002608/http://www.titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2017-234%20sgb.pdf
  • Notes / Alerts
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Turkey.
  • Extra notes in the data

Device

Smart Flex Vascular Stent System

Manufacturer

Cordis a Cardinal Health Company