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.
Model Catalog: (Lot serial: MODEL 31 27 011 SN 6058); Model Catalog: (Lot serial: MODEL 31 27 011 SN 6038); Model Catalog: (Lot serial: MODEL 31 27 011 SN 6018); Model Catalog: (Lot serial: MODEL 31 27 011 SN 6014); Model Catalog: (Lot serial: MODEL 97 85 023 SN 1033); Model Catalog: (Lot serial: MODEL 97 85 023 SN 1034)