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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Veridex llc has received a report that a patient's demographics were incorrectly associated with another patient's identification (pid) number. internal investigation determined that while editing sample information (e.G. sample position 3) an operator selected a patient identification (pid) number for a sample in a different location (e.G. sample position 2) and inadvertently revised the incorrect patient's demographics. the results associated with each pid were correct.