Safety Alert for Electromagnetic defibrillation electrodes for medical apparatus (HR501)

According to Ministry of Health, this safety alert involved a device in Lithuania that was produced by RADIAN Corporation Ltd., South Korea.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Event Number
  • Date
  • Event Country
  • Event Source
  • Event Source URL
  • Notes / Alerts
    Data from Lithuania is current through December 2018. All of the data comes from the Ministry of Health, 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 Lithuania.
  • Extra notes in the data
  • Reason
    Medical devices do not bear the ce marking and the number of the notified body (not in accordance with the requirements of articles 38, 39 and 40 of the regulation).
  • Action
    Do not allow to enter the Lithuanian market


  • Manufacturers representative
    UAB Paramedica Lithuania
  • Source