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 dxh sms systems generates an incorrect "invalid delimiters" message when the host transmits the minimal header record. when this issue occurs the dxh sms does not store the test order in the worklist which results in the specimen being processed by a default order or skipped (when no default order is selected at the system manager).