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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A portion of sps tubes from lot 6090812 were incorrectly labeled at the case and shelf pack level. impacted product will have incorrectly labeled packaging that includes a label for acd tubes catalog number 364606. individual sps tubes are not impacted as the unit level product is correctly labeled. the issue only pertains to the case and shelf pack labelling.