I know there are some changes in the inspection of seed grain and the way that's done, actually moving to a private sector model that is available 24-7 as opposed to CFIA. If CFIA does it, they're going on a cost-recovery basis. I've not seen any kinds of numbers that show 15 times more, as you're recording. I'd be happy to talk to your farmer—through you, if you desire, Mark—to make sure he's not being sold a bill of goods. There are some changes, but nothing that I've seen shows it at that level. I'll certainly check that out for you.
On spent fowl, we're working with Canadian Border Services with regard to the line item that pertains to spent fowl. There is one that says it's fine to bring it in. What we're finding, though, is that spent fowl is coming in, as you rightly point out, in a volume that says it's a lot more than just chicken nuggets, soups, and so on, where it was originally destined to go. It's starting to show up as full-fillet cuts on store shelves, which is not acceptable and not part of what's happening. The package is being put together. We're working with the Chicken Farmers of Canada on how we get on top of that and start to get it back to the flow of where it's supposed to be going.
It's very similar to the pizza kits issue, the cheese compositional standards, as I outlined today in question period, the other issues that we've dealt with and have resolved on behalf of the SM groups. We'll do the same thing on spent fowl. We're in the midst of that assessment right now, working with the Chicken Farmers of Canada and so on.
On PED, when it first was discovered in Canada, CFIA undertook.... I mean, it's under provincial jurisdiction. It's not a reportable disease, so it doesn't go to the federal level. But we assigned CFIA to help their provincial colleagues as much as they could. They undertook work with the provinces to oversee how our biosecurity system was working. They then also started to look for causes, how it was transmitted. The U.S. had done some work on feed inputs and had not come up with any kind of conclusive results to say it was part of it or it wasn't part of it. There was really no rationale in that regard.
CFIA undertook a number of studies and did testing over the ensuing weeks and months, working with a product coming out of the U.S.—blood plasma, a protein enhancement. It is pork blood dehydrated down that is used as a pig starter, for piglets. They thought, since it's affecting the piglets themselves, maybe that was part of the problem. We know it's transferred through the feces. We know that grown hogs will suffer a couple of days with flu-like symptoms, but it doesn't dehydrate them to the point where it kills them, as it does the young pigs.
They did all this testing in the lab in Winnipeg. They found positive PED in the blood plasma, but it did not translate into the finished feed product. No one feeds raw blood plasma to the pigs. There's a process where it goes through another heat treatment and different things. I can get you that scientific rundown. In the final feed result, they never did find a positive. Part of the work that's done in creating the product out of the blood plasma said...you know, it was negated.
We've shared those test results with the U.S. Now that the European Union, led by France, has put a ban on any product...mostly genetics and so on, on Canadian pork, we've shared that science with them as well.