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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Trilogy ventilators with software versions 13.2.04 13.2.05 14.0.00 or 14.1.01 are susceptible to an inadvertent change between prescriptions. this may occur under a particular set of operating conditions and after a specific sequence of key presses without requiring confirmation of the change by the user. affected devices continue to accurately display the active prescription in the upper left hand corner of the display. as this prescription change was unintended and no confirmation was required the user may be unaware of this change.