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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Vision rt has been notified that unintended changes can be made to planned couch parameters specifically the couch rotation parameter during patient set-up. this can occur when a user sets a different couch rotation from the plan couch rotation while performing patient alignment with vision rt's alignrt device prior to treatment with varian's truebeam radiotherapy delivery system [truebeam]. neither vision rt nor varian received any report of patient harm due to this issue.