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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To inform customers that specific product code / lot number combinations may be at risk of having issues related to proper functioning of the device. this includes difficulty with priming and firing failure to obtain tissue sample and in some instances self-activating after priming.