Recall Or Safety Alert for "TAC MX 16-cuts" tomographic systems, models 728131 and 728132, with software version 1.1.3, manufactured by Philips Healthcare, USA.

According to Agencia Española de Medicamentos y Productos Sanitarios (Via FOI), this recall or safety alert involved a device in Spain that was produced by Philips Healthcare.

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
  • Date
    2015-05-25
  • Event Country
  • Event Source
    AEMPSVFOI
  • Notes / Alerts
    The data from Spain is current through June 2018. All of the data comes from Agencia Española de Medicamentos y Productos Sanitarios, 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 Spain.
  • Extra notes in the data
  • Action
    Possibility that the TAC MX-16 cuts systems, with software version 1.1.3, manufactured by Philips Healthcare, USA, do not show the images when they are used in dental applications in studies with the inclined gantry

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    AEMPSVFOI