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 6967830 SN 2256); Model Catalog: (Lot serial: MODEL 6967830 SN 2485); Model Catalog: (Lot serial: MODEL 6967830 SN 2487); Model Catalog: (Lot serial: MODEL 6967830 SN 2481); Model Catalog: (Lot serial: MODEL 6967830 SN 2312); Model Catalog: (Lot serial: MODEL 6967830 SN 2451); Model Catalog: (Lot serial: MODEL 6967830 SN 2313); Model Catalog: (Lot serial: MODEL 6967830 SN 2455); Model Catalog: (Lot serial: MODEL 6967830 SN 2450); Model Catalog: (Lot serial: MODEL 6967830 SN 2519)