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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Due to a production fault in a specific production lot of the triple-focus x-ray tube assembly there is a possibility that the "small focus" may fail. if this occurs no further radiation release will be possible from this focus source. the "large focus" and "microfocus" will still be operational. this malfunction occurs only sporadically and is not a systematic fault.