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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Draeger has become aware of information suggesting that the use of the auxiliary common gas outlet (acgo) at anesthesia workstations of different manufacturers was not performed as described in the instructions for use of the relevant manufacturer and not according to pubiished safety guidelines (pre-use checklist) from various anesthesia societies.