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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Certain types of electri-cord manufacturing company power cords used with medical devices sold by philips healthcare resuscitation patient monitoring respironics and dixtal may be defective in that the power cord's prongs may crack and fail at/or inside the plug. the issue affects medical device ac power cords equipped with a plug that has a prong and ground-pin insert design and a black plastic bridge connecting the terminal prongs on the plug ("taller bridge" design). medical device power cords that do not have a black bridge connecting the terminal prongs on the plug are not affected.