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 product code etched onto the outer box of the above named product contains a typographical error. the code reads "apr2-10" instead of "arp2-10". the product code on the immediate product container (vial) is accurate as is all other labelling accompanying the product.