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 22 16 919 SN20171); Model Catalog: (Lot serial: MODEL 22 16 919 SN20414); Model Catalog: (Lot serial: MODEL 22 16 919 SN20439); Model Catalog: (Lot serial: MODEL 22 16 919 SN20434); Model Catalog: (Lot serial: MODEL 27 93 037 SN22028); Model Catalog: (Lot serial: MODEL 27 93 037 SN22011)