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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Kerr corporation received complaints that the herculite ultra product may be difficult to extrude or may not perform as intended. the composite does not extrude easily. any composite extruded was determined to exhibit signs of dryness and was not workable upon manipulation.