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: 320817 0300 000 (Lot serial: version under 1.4); Model Catalog: 320817 0300 000 (Lot serial: POLO and OPASS software); Model Catalog: 320817 0300 000 (Lot serial: S/N 873110); Model Catalog: 320817 0301 114 (Lot serial: versions under 1.4); Model Catalog: 320817 0301 114 (Lot serial: POLO and OPASS software); Model Catalog: 320817 0301 114 (Lot serial: S/N 873112)