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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Angiodynamics is recalling product that has the potential to contain an ecg clip cable that was not properly manufactured. the affected product is not soldered per specification and may result in the device not properly conducting the ecg signal. angiodynamics began distributing product affected by this recall on february 19 2015.