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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1. in artis systems with a100plus or a100g generators an attempt to resume operation following detection of fault (such as a short circuit in the x-ray tube) can result in the failure of a module in the high-voltage generator. 2. for biplane systems delivered with software version vd11b since april of this year software problems in conjunction with the graphics card may in rare cases result in the loss of image display in the examination room.