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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The ct/mr fletcher set is designed for gynaecological brachytherapy (radiation therapy) and mainly intented for the treatment of the cervix. during tests done at a customer site it has been revealed by the customer's physicist that there is a slight deviation in the accuracy of the dwell position of the source.