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 healthcare diagnostics is conducting a field action for damaged power supply adaptors that are used in the clinitek status clinitek status+ and clinitek status connect systems which can result in an increased potential for electric shock to the user. this also includes orderable spare parts. siemens is providing information regarding this issue in an urgent field safety notice issued to customers.