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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For patients with fill volume of 500mls or less a drain phase ends once the flow rate is less than 25 mls/min for at least one minute although these patients may normally drain slower than 25 mls/min.