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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1) a cable inside the c-arm of systems affected may break within the specific serial number range of 1000 - 1132. a cable break may cause restricted functionality or even failing of the system. an ongoing procedure may be terminated at this system. 2) a cable inside the c-arm of systems within the serial range of 1000 - 1599 may have been routed in an inappropriate manner. without additional measure there is potential that a cable inside the c-arm may break. the problem will not occur systematically but sporadically in the ongoing life time of a system.