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 recall was initiated due to recent tests that indicated some midas touch needle electrodes with modified tip might have an insulation breach and could generate a risk of superficial burn to the patient and/or end-user.