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 has become aware that if multiple quinton stress ecg records are being processed during iecg import at the same time it is possible that the xml patient id from one patient can be incorrectly linked to a report from a second patient that is in the processing queue.