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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In intellispace pacs 4.4 system there is feature which allows the optional configuration of auto export of resolved study exception immediately after resolution. philips has become aware that when this configuration is used it is possible for a system timing issue to occur when exporting data to 3rd party devices. if this system timing issue occurs when demographics are updated such as during exception resolution and the study is immediately exported the patient demographic information can be incorrect in the exported data.