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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In the softbank order entry window or the order modify window keystroke sequence between active and inactive windows while placing a blood product order can cause field validation to fail and the default crossmatch test may be omitted.
Model Catalog: V.25.2 (Lot serial: V. 1.3.0.X); Model Catalog: V.25.3 (Lot serial: USED WITH SOFTSCAPE GUI); Model Catalog: V.23.1 (Lot serial: USED WITH SOFTSCAPE GUI); Model Catalog: V.23.2 (Lot serial: USED WITH SOFTSCAPE GUI); Model Catalog: V.25.0 (Lot serial: USED WITH SOFTSCAPE GUI); Model Catalog: V.25.1 (Lot serial: USED WITH SOFTSCAPE GUI); Model Catalog: V.25.2 (Lot serial: USED WITH SOFTSCAPE GUI); Model Catalog: V.25.3 (Lot serial: V. 1.2.0.X); Model Catalog: V.23.1 (Lot serial: V. 1.2.0.X); Model Catalog: V.23.2 (Lot serial: V. 1.2.0.X); Model Catalog: V.25.1 (Lot serial: V. 1.3.0.X); Model Catalog: V.25.0 (Lot serial: V. 1.3.0.X); Model Catalog: V.23.2 (Lot serial: V. 1.3.0.X); Model Catalog: V.23.1 (Lot serial: V. 1.3.0.X); Model Catalog: V.25.3 (Lot serial: V. 1.3.0.X); Model Catalog: V.25.2 (Lot serial: V. 1.2.0.X); Model Catalog: V.25.1 (Lot serial: V. 1.2.0.X); Model Catalog: V.25.0 (Lot serial: V. 1.2.0.X)