Safety Alert for Massage tables

According to Ministry of Health, this safety alert involved a device in Lithuania that was produced by Not specified.

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
    Only the outer packaging of medical devices bears the ce conformity marking, but the ce marking is not affixed to the medical device itself (does not meet the requirement of article 38 of the regulation); the label of the medical device does not contain information on the manufacturer and the manufacturer's authorized representative in the european economic area (does not meet the requirements of annex 1, paragraph 14.3.1 of the regulation); the batch / serial number of the medical device is not specified (does not meet the requirement of annex 1, paragraph 14.3.4 of the regulation).
  • Action
    Not allowed to enter the Lithuanian market



  • Manufacturers representative
    UAB Urmo Group
  • Source