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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After a functional check of the brakes on the artis zeego system there is a possibility of any output system information being overlaid with different system information. the overlaid information requests users to contact the service department. the system remains operational but the rotary arm can only be moved at a reduced speed.