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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In aquilion 64-slice systems when used in combination with vhp (chvh-001a) which is an optional software for aquilion systems a software problem exists that can prevent scanning from being performed at the specified helical pitch. the problem occurs in aquilion 64-slice systems with vhp software.