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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This recall results from complaints received in the united states regarding the detachment of the healon endocoat opthalmic viscoelastic device (ovd) finger grip. an advisory notice is being disseminated to customers to re-emphasize proper techniques for the use of the syringe included in the healon endocoat directions for use (dfu).