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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There is an issue on cobas it middleware where the masking of tests function (block release) is not working for modules if the master instrument is selected therefore a remote probability that a delay or incorrect initial diagnosis may occur.