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.
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Incorrect label- the label on the back of the device may show model 2500a rather than model 2500 where 'a' indicates the device has alarm functions.
Model Catalog: (Lot serial: 500218376); Model Catalog: (Lot serial: 500222555); Model Catalog: (Lot serial: 500222564); Model Catalog: (Lot serial: 500222578); Model Catalog: (Lot serial: 500222524); Model Catalog: (Lot serial: 500222526); Model Catalog: (Lot serial: 500218362); Model Catalog: (Lot serial: 500218363); Model Catalog: (Lot serial: 500218364); Model Catalog: (Lot serial: 500218366); Model Catalog: (Lot serial: 500218369); Model Catalog: (Lot serial: 500218370); Model Catalog: (Lot serial: 500218373); Model Catalog: (Lot serial: 500222543); Model Catalog: (Lot serial: 500222553)