Events

Recall Or Safety Alert for Surgical table extension device MAGNUS

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 Maquet GmbH.

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
    2016-03-01
  • 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
    Rectification of the recommendations made in December 2015 by the manufacturer Maquet GmbH, Germany, for the users of certain serial numbers of the extension device 1180.19A0 of the MAGNUS surgical table, in relation to the possible fall of the device when it is incorrectly handled.

Device

Surgical table extension device MAGNUS

Manufacturer

Maquet GmbH
  • Manufacturer Parent Company (2017)
    Getinge AB
  • Source
    AEMPSVFOI