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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Due to a memory issue a warning message about unexpected error and possible incorrect data integrity is shown to the user. a reboot of the workstation computer after having received the warning message prevents the issue from occurring. in one instance the warning instructions were not followed and resulted in the image of one patient being archived in another patient's record.