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 was notified by the supplier of the articulated arm that there was the potential for the weld seam between the main stud and the two flaps on the articulated arm to fail. the main welding process to manufacture the joint was not executed correctly and the weld may not be in the correct location.