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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Feedback from a hospital indicated that two neuron delivery catheter 053's received on an order were labeled pnd6f10512 (lot f37120) on the outer product box but the device labeling on the pouch inside the box read pnd6f1056m (lotf37125). it was determined that devices inside pouches are pnd6f10512 devices consistent with the outer product box label.