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 was received from supplier correctly labelled as 16i15. but on receiving at pharmasystems warehouse the "i" in the lot number was misread as "l" in lower case and the master shipping carton and inner storage carton were labelled as 16l15. this wrong lot number was used to enter the product into the system and on customer documents. the actual product and the immediate packaging used to sell the product to consumer was labelled correctly.