I think it's important to stress for the record that of 350 cases, 347 were voluntary recalls, and three were companies that were non-compliant with the voluntary recall and essentially are no longer in business. I think it's important for the record to state that.
I want to come back to you, Ms. Callard. There were two things you said in your testimony that I thought were very interesting.
First, similar products in the United States have the label that they are not FDA-approved. In Canada, they seem to be approved by Health Canada, and the Zonnic example is one of them. Is there anything we can learn from the U.S. example?
Second, you talked about an integrated nicotine framework, which, as we go through the witness testimony, is something that is clearly lacking. What do you think that would look like at the national level?