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 has identified a potential reporting error with the clinitek novus analyzer. if the report clarity setting is disabled there is a potential for the specific gravity leukocytes albumin p:c ratio and/or the a:c ratio to be misreported. this issue impacts systems on sw versions 1.1 and 1.2.