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 # 12 25 023 SN1026); Model Catalog: (Lot serial: Model # 35 22 005 SN1056); Model Catalog: (Lot serial: Model # 12 25 023 SN1006); Model Catalog: (Lot serial: Model # 35 22 005 SN1055); Model Catalog: (Lot serial: Model # 35 22 005 SN1018)