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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There is a highly sporadic malfunction that concerns the 3d reconstruction functionality of the somatom systems. this problem may occur during the process of a 3d reconstruction job planning and editing within a specific funtionality while another functionality ("preview image") is activated. the problem presents itself as an error message window and the system needs to be rebooted.
Model Catalog: 77 40 769 (Lot serial: VA34 OR VA40); Model Catalog: 77 40 769 (Lot serial: SOFTWARE VERSION VA20 VA27); Model Catalog: 77 40 769 (Lot serial: ANY SERIAL NUMBER RUNNING); Model Catalog: 10430603 (Lot serial: VA34 OR VA40); Model Catalog: 10430603 (Lot serial: SOFTWARE VERSION VA20 VA27); Model Catalog: 10430603 (Lot serial: ANY SERIAL NUMBER RUNNING); Model Catalog: 8098027 (Lot serial: ANY SERIAL NUMBER RUNNING); Model Catalog: 8098027 (Lot serial: SOFTWARE VERSION VA20 VA27); Model Catalog: 8098027 (Lot serial: VA34 OR VA40)