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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Prior to nov 1998 safety alert it had been determined that there had been a total of 8 complaints related to improper installation of mechanism spring. complaint date ranged from dec 96 to aug 98. no can comp.