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 there is a low likelihood of incomplete engagement of the spring arm circlip during service or replacement of the spring arm. if the spring arm circlip is not fully seated the spring arm could separate and fall along with the surgical lights monitors or navigation cameras mounted to the end of the spring arm.