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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Bd has identified potential risks with the alaris system model 8100lvp. while the pump is infusing the system may indicate that an air-in-line (ail) alarm has occurred when no air is in the line. these false ail alarms can be attributed to a faulty ail sensor.