Events

Field Safety Notices about GDC

According to Swiss Agency for Therapeutic Products, this field safety notices involved a device in Switzerland that was produced by Stryker Neurovascular.

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
    Vk_20131203_07
  • Event Date Posted
    2013-12-09
  • Event Country
    Switzerland
  • Event Source
    SATP
  • Event Source URL
    https://fsca.swissmedic.ch/mep/#?q=Vk_20131203_07
  • Notes / Alerts
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Extra notes in the data

Device

GDC
  • Model / Serial
    see FSN | see FSN
  • Product Description
    MD: Catheter, intravascular occluding, temporary; Intravascular microflow catheter; Neurovascular embolization implant; Stent, vascular
  • Manufacturer
    Stryker Neurovascular

Manufacturer

Stryker Neurovascular
  • Manufacturer Parent Company (2017)
    Stryker
  • Source
    SATP