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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Access cea may generate erroneously low cea values after samples have been frozen. product insert directs customers to freeze samples if assay will not be completed within 48 hours or for shipment of samples.