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 reasons to believe that in some cases the combi dockable table neurosurgery may have a manufacturing defect. in certain cases a potential risk of a sudden drop in table height may exist. this can happen with or without user interaction and may occur unexpectedly. the maximum drop in height is 5 cm. to address this issue siemens will inspect and correct any affected devices on site.