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 company has become aware that there is the potential that over time a buildup of surgical waste on the receptacle bearing surfaces may increase the force required to rotate the suction manifold. if the force becomes too high the manifold cannot be rotated - therefore it cannot be inserted or removed. once this occurs there will be no vacuum applied to the suction manifold so the primary function of the affected rover canister is lost.