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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Siemens has become aware that it is possible for patients or operators to have their fingers trapped and pinched between the table top and the bottom frame of the 550 txt treatment table which is part of the affected systems listed in section 64(a). secondly and unrelated siemens received a report on an incident in which a cable inside of the 550 txt treatment table had been damaged due to contacting a moving part. the resulting short-circuit caused overheating of an electronic circuit board inside the table base.