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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During steam sterilization validation it was discovered that the trident constrained liner impactor tips do not meet the required sterility assurance level (sal) of 10-6. please note that these instruments are sterilized at the hospital prior to surgery however and do not come from stryker sterile.