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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Ige calibrator series ie2492 lot 387-392ie value assignment has now been aligned to the 3rd international standard for human serum ige 11/234. turbidimetric (non-ifcc cal.) quality control targets and ranges now apply.