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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The tecnis 1-piece intraocular lenses (iols) are being recalled because the haptics of some tecnis 1-piece iols (model zcb00) have adhered to the lens optic after insertion into the eye. this situation can lead to additional manipulation to separate the haptics from the optic during surgery which could lead to an injury.