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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A fault has been identified with the pressure lines-in some instances a partial occlusion of the pressure elbow has been found.
Model Catalog: RT130 (Lot serial: 040701 to 041216); Model Catalog: RT131 (Lot serial: 040701 to 041216); Model Catalog: RT235 (Lot serial: 040701 to 041216); Model Catalog: RT236 (Lot serial: 040701 to 041216)