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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Philips has become aware that when hl7 lab messages are sent to a piic ix system that has been localized forcomma delimiters the lab result is incorrectly displayed on the bedside monitor. an expected delimiter isstripped from the lab value and the number shown is of a higher magnitude than expected. if lab results areincorrect a clinician may initiate incorrect treatment or delay necessary treatment this problem only happenswhen the piic ix is configured during set up for regional settings where the delimiter is a comma. the laboption must be in use and the workflow utilizes the automatic lab interface displayed at the bedside monitor.