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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Manufacture has reported discovering quench lines installed by the system owner which do not meet the specifications provided. if the quench line is not installed properly or is restricted or obstructed when a quench occurs it could cause helium gas to vent directly into the mri room or other areas.