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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The connection bracket shows too much machanical play at the operating room table interface for some procedures. the cause of this play is that the hole in the lock washer which is responsible for locking the accessory to the operating room table interface is too large.