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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When the drain ends in a "no flow" condition the home choice system may not record a small portion of the actual volume of fluid drained during the cycle as much as 10 mls or 1% of the volume of fluid.