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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Centricity laboratry instrument interface to data innovations (di) is processing a preliminary result instead of the final result from the process manager (psm). when psm reruns (repeats) a test the psm sends bothpreliminary and final results in the same result message but only the preliminary result is filed and reported.