Field Safety Notices about Accu-Chek Inform II Base Unit, Handheld Base Unit, cobas h 232 POC system, cobas h 232 POC system (scanner version), CoaguChek Pro II Kit (WLAN), CoaguChek Pro II Kit (no W-LAN), CoaguChek XS Pro system, CoaguChek XS Plus system, Accu-Chek Inform II system (W-LAN), Accu-Chek Inform II system (no W-LAN)

According to Ministry of Health, State Institute for Drug Control, Coordination Center for Departmental Medical Information Systems, this field safety notices involved a device in Czechia that was produced by Roche Diagnostics GmbH.

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
  • Date
  • Event Country
  • Event Source
  • Event Source URL
  • Notes / Alerts
    Czech data is current through July 2018. All of the data comes from the Czech Public Registry of Medical Devices, 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 data from the U.S. and the Czech Republic.
  • Extra notes in the data