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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During the acquisition of the slide the system may skip spots during a run. the acquisition stops on one spot of an acquisition group and then jumps to the next acquisition group available (if it exists) without any error message to the user. in case of skipped spots no results are displayed by myla and no error message appears.