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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This field action has been initiated due to the inappropriate shipment of four revolve units to a canadian hospital. the user manual included with the product contains a change to remove neurosurgery application that's not yet approved by health canada.