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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The cobas it middleware software rule engine provides a rule trigger based on tests in profiles. this software also provides the possibility to configure profile within profile. when a profile within profile is used as a rule trigger the rule will not be triggered for tests in the sub-profile. any action in the affected rule (e.G.Block release modify results) will not be performed.