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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Philips healthcare has become aware that a software issue may cause misdiagnosis when using the uniform resource locator (url) pacs integration. when loading a study to an analysis application while using url pacs integration configuration after another study was opened by a review application the analysis monitor is updated with the study of the current patient but the review monitor continues to display the study from the previous patient.