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 stryker neptune waste management system is intended to be used in the operating room pathology surgical centers and doctor's offices to collect and dispose of surgical fluid waste as well as to collect smoke generated from electrocautory or laser devices. stryker instruments was made aware was made aware through informal reports from hospital personnel that a death had occurred and possibly related to use of a neptune rover. the root cause of the problem was confirmed not to be caused by a product malfunction or the result of a non-conformance but rather the event resulted due to a use error.