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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There is a potential issue between the cobas it middleware system and customer laboratory information system (lis) when spaces are used in the sample id's. if the lis sends sample id with leading spaces to citm this id will be saved with spaces when an instrument sends results back to citm since the driver removes these spaces during the transmission therefore sample id not found or wrong sample id association may occur.