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 single reconstructed ecg lead printed or viewed at the information center ix system may be misrepresented in the presence of certain combinations of primary and secondary lead for analysis. these include leads i and iii leads iii and avf and leads i and avr. following are the lead combinations that are affected: -lead i and lead iii are used to derive the avl lead (incorrectly derived) -lead i and lead avr are used to derive the avl lead (incorrectly derived) -lead i and lead avr are used to derive the avl lead (incorrectly derived).