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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In rare circumstances the lh 700 series and gens hematology analyzers may incorrectly gate the neutrophil cell population on patient samples. some of the neutrophils may be included in the eosinophil population.