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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Stryker has become aware that periodic testing normally completed during the manufacturing process was not conducted for products manufactured between march 28 2014 and may 2 2014. changes to the quality of the weld during this period may not have been detected and may be less effective than intended.