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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There is a potential for lenses with reduced ion permeability values to have reduced movement on the eye resulting in sympthoms similar to a foreign body sensation.
Model Catalog: (Lot serial: 6644234 TO 6721274); Model Catalog: (Lot serial: 6642132); Model Catalog: (Lot serial: 6642109); Model Catalog: (Lot serial: 6637103); Model Catalog: (Lot serial: 6626127); Model Catalog: (Lot serial: 6637019); Model Catalog: (Lot serial: 6642119)