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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Siemens is issuing control console update version 9.2.18 for digital linear accelerators of type primus (primus hi mevatron primus & mevatron primus plus) and oncor (oncor expression & oncor impression plus) to fix a number of safety issues: cumulative positioning errors electron or stereotactic treatments with the reticle inserted delayed error message in ultrafast imrt treatments and incorrect verification of the beam shape when using non-syngo primeview.