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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There is a negative bias in addition to that which was communicated in december 2010 for samples with insulin values below 10 uiu/ml and an increased imprecision compared with the representative data provided in the instruction for use for these kit lots.