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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Echocardiography volume measurements that were performed within crs were not reflected correctly in associated results management (rm) reports. this occurred when echocardiography volume measurement data was not saved correctly within the crs persistence data and in the rm database. the issue was caused when point-trace mode was enabled in crs a feature that was introduced in crs 2.12.05. a software upgrade to crs 2.14.03.Su2 will be made.