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 a small number approximately 6% of 125-dihydroxy vitamin d ria kits containing calibrators d lot 34649 and e lot 34650 similar cpm values for both calibrators are obtained. these abnormal results lead to an incorrect calibration curve fit.