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 27 98 705); Model Catalog: (Lot serial: MODEL 11 03 006); Model Catalog: (Lot serial: MODEL 16 00 209); Model Catalog: (Lot serial: MODEL 11 06 900); Model Catalog: (Lot serial: MODEL 27 98 606); Model Catalog: (Lot serial: MODEL 86 12 590)