Events

Recall Or Safety Alert for MultiDiagnost Eleva systems, product code 708032, and MultiDiagnost Eleva with flat panel detector (FD), product code 708034, 708037 and 708038

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 Medical Systems Nederland.

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
    2016-08-11
  • Event Country
    Spain
  • 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 C-arm of the MultiDiagnost Eleva and MultiDiagnost Eleva FD systems, manufactured by Philips Medical Systems Nederland, BV, Holland, can move freely in the lateral direction and beat forward.

Device

MultiDiagnost Eleva systems, product code 708032, and MultiDiagnost Eleva with flat panel detecto...

Manufacturer

Philips Medical Systems Nederland
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    AEMPSVFOI