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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Due to a potential manufacturing error a rare possibility exists for a sudden drop in table height of the patient table. the maximum drop in height is 5cm and this error could potentially occur with or without user interaction. therefore it is necessary to inspect the table of distributed systems to ensure it was manufactured in a manner that confirms safe operation.