Recall Or Safety Alert for Device x-ray angiographic multi-axis Artis zeego

According to Ministry of Health of the Republic of Belarus, this recall or safety alert involved a device in Belarus that was produced by Siemens AG Medical Solutions Business Unit AX, Germany.

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
    Recall / Safety alert
  • Event Number
    ИМ-7.98031
  • Date
    2014-09-22
  • Event Country
  • Event Source
    MHRB
  • Event Source URL
  • Notes / Alerts
    Belarussian data is current through June 2016. All of the data comes from Health Canada, 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 Belarus.
  • Extra notes in the data
  • Reason
    The manufacturer has determined that there is a potential problem with the device running software version vc21b (serial numbers 10094135, 10094137, 10094141, 10280959) in combination with a large display, under certain circumstances, radiation radiation may be blocked. the manufacturer began work on changing the software and sent a notice to all users, identifying: the product, the problem and the subsequent actions of the users. in case of problems, it is recommended that everyone contact the local representatives of the manufacturer.

Manufacturer