Recall Or Safety Alert for 708032: MultiDiagnost Eleva - 708033: UroDiagnost Eleva - 708034: MultiDiagnost Eleva with Flat Detector - 708035: MultiDiagnost Eleva with Flat Detector - 708036: MultiDiagnost Eleva - 708037: MultiDiagnost Eleva with Flat Detector - 708038: MultiDiagnos

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 N/A.

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
  • Event Country
  • Event Source
  • Event Source URL
  • 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
    Safety warnings in relation to the possible breakage of the fixation of the upper and lower part of the mechanism that controls the tilt of the system with the possibility that the table rotates at high speed, which could potentially cause the patient to fall from the table .


  • Source