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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Teleflex medical has issued a recall due to the possibility that the intake port may be blocked which can cause the bag to fail to fill. no patient injury or harm has been reported however a delay in treatment may occur while another resuscitator is obtained. a delay in treatment may potentially lead to adverse consequences such as hypoxia.