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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A button on the hand controller on the precedence and skylight spect systems may become stuck which may result in unintended motion of the detector which could cause the detector to come in contact with the patient if the operator is not diligently observing the scan.