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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A temperature excursion occurred during a single shipment of 18 shelf packs of product 215228 lot 5106520 to a single customer. due to the sensitive nature of the formulation it was recommended that the product involved in this specific shipment be discarded.