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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Manufacturer advises that a specific scenario has been identified that causes patient demographics data (patient name age sex) from the previous order received from the laboratory information system(lis) to be merged with the next order. the incorrect patient demographics data will display on the advia centaur/advia centaur xp user interface print on instrument-generated reports and will be transmitted to the lis with the test result.