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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Inaccurate results reported to the system when a sample is diluted and placed back into the system without assigning the sample a unique different sample id. as a result patient sample results may be reported with an incorrect result value resulting in inaccuracy imprecision or error comment reports together with the result.