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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On some units of mpr the duckbill valve and retention ring inside the patient valve housing may become dislodged and fall into the mpr bag/body. if this were to occur the mpr may loose its ability to generate the positive pressure necessary to function properly.