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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Smiths medical has issued a field safety corrective action for certain single limb circuits for pneupac ventilators with peep valve because they are labelled as "mr conditional" but contain peep valves that should have been labelled as "mr unsafe". if the affected products are used in an mr environment there is a potential for the peep valve to become dislodged during the mri procedure or for artifacts to be created in the mri scan.