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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Issue with the l3 inductor (specific lot) a component of the v60 ventilator power management (pm) printed circuit board (pcb). the source of odor/burning smell was due to the thermal damage on the l3 inductor on the pm pcb.