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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When users clicks on window grid header before selecting a blood product for order no field validation is performed. transfusion can occur without compatibility testing performed.
Model Catalog: V.23.2 (Lot serial: v. 1.3.0.4 - 1.3.0.5); Model Catalog: V.23.1 (Lot serial: v. 1.3.0.4 - 1.3.0.5); Model Catalog: V. 23.0 (Lot serial: v. 1.3.0.4 - 1.3.0.5); Model Catalog: V.25.1 (Lot serial: v. 1.2.0.7 - 1.2.0.15); Model Catalog: V.25.0 (Lot serial: v. 1.2.0.7 - 1.2.0.15); Model Catalog: V.23.2 (Lot serial: v. 1.2.0.7 - 1.2.0.15); Model Catalog: V.23.1 (Lot serial: v. 1.2.0.7 - 1.2.0.15); Model Catalog: V. 23.0 (Lot serial: v. 1.2.0.7 - 1.2.0.15); Model Catalog: V.25.1 (Lot serial: Used with SoftScape Gui); Model Catalog: V.25.0 (Lot serial: Used with SoftScape Gui); Model Catalog: V.23.2 (Lot serial: Used with SoftScape Gui); Model Catalog: V.23.1 (Lot serial: Used with SoftScape Gui); Model Catalog: V. 23.0 (Lot serial: Used with SoftScape Gui); Model Catalog: V.25.1 (Lot serial: v. 1.3.0.4 - 1.3.0.5); Model Catalog: V.25.0 (Lot serial: v. 1.3.0.4 - 1.3.0.5)