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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Bd has confirmed a limited number of tubes associated with the lots listed and currently in the market may exhibit stopper pullout where the stopper is withdrawn from the tube as the user removes the needle from the stopper following specimen collection.