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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Interruption in central water delivery system resulted in a loss of water pressure causing negative pressure in water system compared to hemodialysis machine. this allowed disinfectant from machines to contaminate the central water delivery system and storage tank.