Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
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If the system is not turned off manually at regular intervals an automatic reset of the large display controller can occur. during the reset the system switches for approximately 1-2 minutes into the bypass fluoro mode. during this time only the native fluoroscopic image is displayed.