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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Under certain conditions the isocenter positions and the rt structures exported fron iplan rt dose version 4.1 might be incorrect. as a consequence treatment dose might be delivered to a region different from the planned one.
Model Catalog: 70228A 70228B 70228C (Lot serial: VERSION 4.1); Model Catalog: 70440 (Lot serial: VERSION 4.1); Model Catalog: 70440A (Lot serial: VERSION 4.1); Model Catalog: 21213D 21213E 21213F (Lot serial: (v.4.1.0 4.1.1 and 4.1.2)); Model Catalog: 70214C 70214D 70214E (Lot serial: VERSION 4.1); Model Catalog: 70213C 70213D 70213E (Lot serial: VERSION 4.1); Model Catalog: 21387 21387A (Lot serial: (v.4.1.0 4.1.1 and 4.1.2)); Model Catalog: 21213D 21213E 21213F (Lot serial: VERSION 4.1); Model Catalog: 21387 21387A (Lot serial: VERSION 4.1); Model Catalog: 70440A (Lot serial: (v.4.1.0 4.1.1 and 4.1.2)); Model Catalog: 70440 (Lot serial: (v.4.1.0 4.1.1 and 4.1.2)); Model Catalog: 70228A 70228B 70228C (Lot serial: (v.4.1.0 4.1.1 and 4.1.2)); Model Catalog: 70214C 70214D 70214E (Lot serial: (v.4.1.0 4.1.1 and 4.1.2)); Model Catalog: 70213C 70213D 70213E (Lot serial: (v.4.1.0 4.1.1 and 4.1.2))