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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Plasma collected with lithium heparin may give erratic and unpredictable results when compared to edta plasma when using the integra ammmonia reagent on the cobas integra 400 and 700 analyserx.