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 remote likelihood that the eds light suspension central axis may have an insufficiently assembled joint in the suspension. the eds systems have redundant connections throughout the suspensions. if the eds light suspension central axis falls it could potentially cause serious injuries to healthcare providers and/or patients. to date there have been no adverse events reported for this issue.