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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Stryker endoscopy has become aware that the pneumo sure heated tube set has the potential to display an error message stating "check/change tube set" and then the flow drops to a maximum of 11 liters/minute. if the issue is not resolved pneumoperitoneum may take longer to establish due to the limited flow.