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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Some 491b (p/n 39662) rectal/esophageal temperature probes are not reading correctly causing the blanketrol device which the probes connect to to shut down operation and display a "check probe" error message. when the probe cable the component which connects the probe to the blanketrol device is moved during use the probe intermittently loses continuity causing the probe to inappropriately operate and display/provide wrong temperature values.