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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During use of an iplus unit with software version 1.7 if an error occurs when in any procedure screen the air setting will change to 1% and off. after the error is cleared the air setting will erroneously remain at 1% and off.