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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Health canada notified jtech that tracker freedom was reclassified as class ii because it was an active diagnostic device and the software monitored the patient. a (health canada) letter dated 8-dec-2009 identified the request for notification to be sent to customers.