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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Cardinal health has received communication from our us manufacturer advising us of a voluntary recall initiated for the convertors tiburon arthroscopy drape and convertors under buttocks drape with fluid control pouch ii due to a labelling error. in limited cases the outer label of the drape pouches does not match the drape packaged inside.