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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Under rare circumstances in blood order processing (bop) the qa algorithym failure. "specimen reaction entry does not match system interpretation" is not generated when the reaction result pattern fails to match the reaction result interpretation. this only occurs when resulting user defined test codes containing the character string "rck" (for example btrck1). the system defined percent codes are not affected by this problem.