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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Coopervision has identified two lots of biomedics toric with incorrect axis specifications 10 degrees and 80 degrees respectively. the lots were manufactured in may 2011. based on this information coopervision inc. is initiating a product recall and replacement for the referenced product lots. this recall is being initiated to the wholesale/distributor and eye care practitioner level.