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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Graphic printed board (pcb) installed in stellant ct injection systems included an incorrect component. these systems use the component on the pcb to run the device clock. as a result affected devices are losing roughly one minute per hour of device use.