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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The reason for this recall/correction is to inform users a software issue that requires correction has been found in the demographics manager feature of impax cv software. in specific circumstances a patient's report generated by the demographics manager service may be populated with demographic data from a different patient's report.