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 november 2004 through july 2016) of the dyonics sagittal saw blade due to a labelling issue. the single use affected devices are provided sterile and do not have an expiration date provided on the label.