Alerte Ou Avis De Sécurité sur Biplane cardiovascular X-ray system

Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.

Risk of interruption in treatment/procedure due to an inability to move the table.The table will reboot if users attempt a powered and manual movement at the same time.The reboot will take approximately 90 seconds during which time no motorised movement will be possible. This has led to delay during emergency treatment. Basic imaging will be available.