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 is being initiated by the manufacturer to reduce the chance of a blockage and improve the flow of water and chemical through the nozzle within the unit that would connect the 7th channel in a 7-channel scope to the innova unit. the size of this nozzle is currently 0.2 mm and it will be replaced by a 0.5 mm nozzle.