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 following issue is being addressed by ge healthcare file no. fmi 85442. ge healthcare has recently become aware that a database handling error could occur during the image acquisition process affecting the completeness of acquired images with centricity universal viewer running on a pacs-iw foundation. there is a potential that one or more "image series" (i.E. all images within an image set) may be missing from an exam without a user warning displayed in the viewer. while this is rare this can occur with imaging studies that consist of a very small number of images per series. e.G. cr thorax exam with 1 image per series. there have been no injuries reported as a result of this issue.