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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Power supply fails from mechanical damage such as dropped accidently or teardown of cascade pro system. the power supply met requirements of iec 60601 for medical devices but it was not designed by the manufacturer for the rigors encountered in its actual use environment.