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: 322003 (Lot serial: FOR CAT 322003 - SEE 05 & 06); Model Catalog: 322003 (Lot serial: 2064273 2064256 2071280); Model Catalog: 322002 (Lot serial: FOR CAT 322003 - SEE 05 & 06); Model Catalog: 322002 (Lot serial: FOR CAT 322002 - LOT 2064256); Model Catalog: 322002 (Lot serial: 2064273 2064256 2071280); Model Catalog: 322003 (Lot serial: FOR CAT 322002 - LOT 2064256)