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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Siemens is investigating an issue on the advia 560 hematology system which may cause an incorrect result to be reported. siemens has received two reports of multiple discordant records for the same sample id (sid) in the advia 560 hematology system database that occurred during the installation of the systems. the database should only contain one record of a sample id number for any given time and date. if there are multiple records for the same sample id it is possible that multiple results may be manually or automatically sent to the laboratory information system (lis) printed or displayed on the results report screen.