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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Cobas it middleware feature "sample closing" could fail if a "rebuilt sample" message was sent by the host before the "sample closing date" already established by the user.The sample result mismatch may occur if the customer allows recycling patient's ids and if their system was set to allow "sample rebuild".