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 likelihood that the tc mounted f300 exam light may have tolerance issue with the adapter assembly which could potentially not allow the snap ring (c-clip) to be seated correctly. if this is the case there could be insufficient mount force that may cause the equipment to fall resulting in serious injury.