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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Eclipse oxygen system units may experience premature wear on electrical connector between battery bridge printed circuit board and power manager printed circuit board that could lead to temporary power interruption when operating from power cartridge causing unit to sound an alarm and shut down.