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 lots of the affected lenses did not meet the new manufacturing acceptance limit for the presence of residue (silicone oil) which may cause hazy vision or discomfort severe eye pain or eye injuries requiring medical treatment.