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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Alcon confirmed complaints for the 23g non-valved trocar cannula and infusion cannula related to a loose fit between the non-valved trocar cannula and infusion cannula. this loose fit may cause the infusion cannula to dislodge from the trocar cannula during the surgical procedure which may eliminate the necessary infusion to the eye required to maintain adequate pressure while operating.