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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Smith & nephew inc. is initiating a voluntary field corrective action/recall of all batches (shipped from september 2013 through october 2016) of the osteoraptor with ultrabraid suture due to a labelling error. the outer box incorrectly states the suture colour as blue the provided suture is white. the inner label is correct.