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 gdna nucleic acid method card (pn: a50088 ln: 023331) and viral na method card (pn: a50090 ln: 023332) contained in the spri-te start up kit (pn: a50094 ln: 023292) are mislabeled. due to this mislabeling the extraction kits used with the gdna and viral na extraction kit method cards will not produce expected quantities of nucleic acid.