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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Teleflex medical have received reports of artifacts being generated in patient monitors. it occurs when the heated wire breathing circuits are used in close proximity to the leads and electrodes of patient monitors and where electrical conductivity has degraded.