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 power on process the therapy parameter section of memory is being corrupted & used for therapy calculations. pumps may over infuse or not run. corrupted rate or dose parameters not in right range.