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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Recall is due to the possibility that the dispensor is mislabeled as "soft n' stretchy light image s-spots (ref# 677)". the risk exists that any confusion could cause concern and the need to re-image if it was to be used on a patient to mark a scar instead of a mole.