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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Maximum pressure relief valve setting is different to the 40 cm water described in the rd1000 operating manual could result in this safety feature not preventing delivery of greater inspiratory pressure to pat.