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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The cp200 has stat electrocardiograph (ecg) mode that generates an ecg without an associated patient identifier and the auto ecg mode where the user can override the required patient identifier.
Model Catalog: CP2-1E1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2AS-1E1-L (Lot serial: SEE MANUFACTURER.); Model Catalog: CP2-1F1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2A-1E1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2A-1F1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2AC-1E1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2AC-1F1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2AS-1E1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2AS-1F1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2C-1E1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2C-1F1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2S-1E1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2S-1F1 (Lot serial: SOFTWARE VERSION 2.4); Model Catalog: CP2SC-1F1 (Lot serial: SEE MANUFACTURER.); Model Catalog: CP2SC-1E1 (Lot serial: SEE MANUFACTURER.); Model Catalog: CP2S-1F1 (Lot serial: SEE MANUFACTURER.); Model Catalog: CP2S-1E1 (Lot serial: SEE MANUFACTURER.); Model Catal