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 has received complaints regarding the 3d tube head of the ysio system moving to the planned and programmed end position faster than expected and then stopping with an error code. a system reboot is then required. this issue is due to a software bug.