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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In the course of product monitoring activities it was found that during the operation of an artis zee / zeego system equipped with generator a 100 plus (material number 10563420) and due to a tolerance problem in the power supply of the generator control above a specific value the generator may fail.