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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Steris corporation has learned that the harmony la/led monitor arm adapters may become unstable when used in conjunction with lead shields or comparable medical devices that exceed the weight and moment limitations of monitor arm adapter. the weight and orientation of these devices may result in suspension system instability and damage to the monitor arm adapters.