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 received reports that when changing the anesthetic gas monitor water trap (m1657b) the manifold seals on the philips gas analyzers models m1013a m1019a and m1026b may be unintentionally removed. a missing seal results in leakage and may cause incorrect monitor readings of inspiratory or expiratory gas levels.