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 incorrect volume for the cunjugate well (r1b) is printed on the access dhea-s reagent outer kit box label. the reagent does contain the correct volume for producing 50 tests.