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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The 4 ml fx sodium fluoride/potassium oxalate tube may have no or low additive (sodium fluoride and potassium oxalate) which can effect analytical results for glucose and lactate.