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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The affected lots contain probes that may produce no audio signal. the lack of audio signal will be apparent to the user once the probe is connected to the doppler transceiver and there is not a reasonable probability that the use of or exposure to the product will cause serious adverse health consequences.