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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An inappropriate cable connection has been assembled in artis zee systems with a certain serial numbers. such an inappropriate cable connection may cause a system failure which may possibly lead to a restricted maneuverability of the gantry system. this update only affects systems of a specific production series.