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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Potential risk when the alaris pca module is used with the alaris pc unit. the alaris pca module can potentially infuse above or below the intended infusion dose for a specific sequence of events syringe volume warning message occlusion warning messagedfu for fluid ingress and dfu for iui connectors.
Model Catalog: 8120 (Lot serial: ); Model Catalog: 8015 (Lot serial: INFORMATION.); Model Catalog: 8015 (Lot serial: A TOTAL OF 4068 SERIAL); Model Catalog: 8015 (Lot serial: NUMBERS-SEE MANUFACTURERS)