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 threads of the outer tube of the shock module of low profile rotate are short which results in insecure assembly. use of the product may cause the patient to fall with continued use as the shock module can become loose from the foot blade.