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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Trumpf has received two customer reports of the leg section of the table articulating without prompting from the user. according to these reports and the analysis conducted thus far this independent movement can occur without particular circumstance or condition. initial findings have led trumpf to assume for the safety of patients and users that unintended movement could occur on any version of titan without notice.