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 printed circuit board assembly responsible for blood pressure measurement and analysis (material number 400387 reffered to as the "mod f" board) includes a capacitor (c600) that was installed backwards. affected devices may intermittently report c02 and c12 error codes which result in the device being unavailable for use.