(11 years, 9 months ago)
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The hon. Gentleman must be careful to distinguish between prosecution and litigation. Civil litigation may follow—I do not know—if there is prima facie evidence. When I responded in the House to an urgent question, I said that it seemed to me, without being in possession of all the facts in Ireland, that there was a possibility of criminality. That is a matter for the Irish authorities, and it would be absolutely wrong of me to assume any responsibility or to encourage the Irish in one way or another in their prosecution policy. However, they will no doubt consider whether fraud has taken place, and trace the perpetrators, whether they are the supplier in Poland, as it seems if their tracing is correct, or the people in Ireland who took receipt of the meat. That is for the Irish to decide, and I cannot interfere in that process. I can only express a view, which I think is shared by many people, that if criminal activity takes place on something as important as the food that people eat, we should use whatever powers are available.
The Minister referred to cross-contamination being a source of trace DNA found in other food products. Does he accept that other meat derivatives, such as protein powders to bulk up products, could be deliberately included in processed food when their origins are unclear, because there is no secure system for labelling and tracking the source of such additives through the supply chain?
It is not uncommon in inexpensive burgers, for example, to use bulking material such as beef protein, and it is not illegal to do so. The EU labelling regime changes to which the hon. Member for Ogmore referred will require such material to be more specifically labelled in future. I agree that it is a difficulty for those who are trying to enforce compliance because it is obviously much more difficult to identify the speciation of a brown powder than a rump steak. The hon. Member for Croydon North points to a difficulty, and we must be aware of it and consider what we can do about it.
I want to deal with some of the broad points that were raised. First, it is simply not the case that the system has been fragmented and, suddenly over the past two years, no one has known what anyone is doing. There was a change in 2010, but the Food Standards Agency has always been the key player in food safety and analysis, including competition. It has always worked incredibly closely with trading standards departments throughout the country which often do the testing at local level. The Department of Health has always had parliamentary responsibility for answering for the Food Standards Agency in response to questions from hon. Members. None of that has changed.
The only change in 2010 was in labelling policy, which was returned from the FSA to the Department for Environment, Food and Rural Affairs because we knew that there would be issues in the EU about country-of-origin labelling and we wanted to have a clear handle on that. Ministers in my Department were inevitably involved in those negotiations. They were going to be advised by civil servants in the FSA or the Department, and it seemed more sensible for them to work with those in the Department. That was the change that was made in 2010, and it does not imply fragmentation of responsibility. There is still a close working relationship between us and the FSA, and I do not think anyone would seriously challenge that or the close working between the FSA and trading standards departments.
Secondly, another charge was that the FSA’s overall budget has been reduced. That is a matter for my colleagues in the Department of Health, but let us be clear that that is not an operational reduction, but a result of the merger with the Meat Hygiene Service, which has produced economies of scale by restructuring support staff and accommodation charges, and enabled us to save money. Saving money is a good thing if it can be done without detriment to the service. We must be clear about that.
Thirdly, there is a feeling that there are vastly fewer trading standards officers around the country and that the service is denuded of capacity. I accept that there are fewer trading standards officers, but the scale of that reduction is nothing like what has been suggested. Local authority returns suggest that on 31 March 2012, 2,709 people were engaged in UK food law enforcement, which is a 2.3% reduction since the previous year, and a 6.1% reduction since 2009-10. I am concerned about that reduction and the priorities that local authorities are choosing to make in what they do because food law enforcement is a key part of their work. I would encourage them to ensure that their priorities are the same as those of residents in their area. However, the reduction in the level of testing is not huge or swingeing.
We sometimes talk about the number of samples taken, but we should distinguish between the number of samples and the number of tests done on them. We are becoming more and more sophisticated in what we can provide. I will give an indication of some of our work in the Department. One policy area is the research that we commission every year into new methods of testing for compliance of foodstuffs. We put £450,000 into that each year.
DNA testing is by no means the only tool available for testing. Stable isotope testing is being developed and is a valuable tool. Proteomics are a key test which is more often used in ELISA—enzyme-linked immunosorbent assay—which gives similar findings of speciation and origin to DNA, but at a lower cost. Metabolomics involves looking at metabolites in food. All those tools are being used to ensure that the service we provide is as effective as possible.
Let us not run away with the idea that we have a supine, inefficient service in this country that never catches anything, and the wonderful Irish can do it, but we cannot. Some of the things that have been found and dealt with over recent years include buffalo milk adulterated with cow’s milk; fruit juice adulterated with sugar and water; maize adulterated with rapeseed oil; the identification of basmati rice from its origin; the speciation of meat and fish, making sure that no offal and blood proteins are in meat products; the origins of beef; traditional breeds—distinguishing between one breed and another—the origin of fish, whether chicken has been previously frozen; and production methods, so whether something is organic, as it says it is on the packet. We test for all those things. We occasionally find non-compliance and we deal with it, so let us get away from the idea that somehow we are either complacent or have ineffective protection in this country.
I hear what the Minister says about the reduced numbers of local authority food safety officers, but will he give us the figure for the reduction in food safety tests carried out? Unfortunately, I do not have the documentation here, but I believe that in the freedom of information request obtained by the trade union, Unison, there was a 30% reduction in tests, which would mean a considerable increase in risk to consumers purchasing burgers or other meat products, not only from supermarkets, but from the many other outlets that operate in that area, and—I will leave it at that.
I was going to move on to the issues about phenylbutazone and horse passports, as that was the other factor that has been referred to several times in the debate.
Let us be clear about phenylbutazone: it is a potentially harmful substance—in fact, there is little evidence one way or another, but we cannot say it is safe. That is why it is excluded from the food chain and it is quite right that it should be. It is principally excluded via the horse passport system. If the horse passport system is being properly applied, it will be excluded at the point of the abattoir. It should not enter the food chain and it should be simply disposed of in other ways. It is not the only drug residue that is occasionally tested for and that we need to be aware of. The Veterinary Medicines Directorate checks for a string of residues that we would also wish to exclude from the human food chain. The evidence from sampling suggests that a small quantity of phenylbutazone is making its way through, in some samples. That is concerning and it has to be investigated, which is exactly what we are doing. The Food Standards Agency is now looking at that in detail to see whether it can get a clearer picture.
There is a problem with the fact that it takes a long time for the test results to come through. I am afraid that I cannot explain why that is, but I am advised that it takes about three weeks to get the results back. During that time, it is entirely possible for food to be passed across the English channel to French markets, where it could enter the food chain. As soon as we have a positive confirmation, we advise the French—or whoever it is—authorities in the same way that they advise us. We have a wonderful network of agencies around Europe. They are constantly in communication and advise one another, which is why we knew about the Irish issue and why we would always notify the French—to ensure that that is the case. However, there is a delay, and the hon. Gentleman raises a point that I accept I need to look at further, to see if there is more that we can do.
Does the Minister not agree that it would make much more sense to prevent the transport of such meat to its destination before the results of the tests for bute have come through? For instance, it could be possible to keep it frozen until it is clear that there is no contamination.
That would require all 9,000 horses that are killed for human consumption—the vast majority of which go abroad, as the hon. Gentleman will appreciate, because there is no appetite for horsemeat in this country, generally—to be kept in cold storage over a period of time while tests are being conducted. That is an option. What we have to do is be proportionate—we are required by law to be proportionate about what we do, because there are costs involved for exporters—and we can only do that if the evidence shows that it is a proportionate action to take. We are collecting that evidence at the moment and I will then take advice. If at any stage, the chief medical officer or the Food Standards Agency advises me that taking any action of that kind is necessary for the protection of human health, I will take it. I have not received that advice at the moment.