Select Committee on Environment, Food and Rural Affairs Written Evidence


Memorandum submitted by Scottish Shellfish Marketing Group Ltd (M3)

BACKGROUND

  The Food Standards Agency has a statutory responsibility to carry out a toxin monitoring programme to satisfy the requirements of EC Shellfish Hygiene Directive 91/492/EEC. The level of monitoring is based by the Agency on a risk assessment of the various inshore and offshore sea areas.

  In Scotland some 70 inshore shellfish sampling sites, primarily aquaculture sites, have been identified by FSAS for monitoring for the programme. The testing of shellfish from these sites is carried out on behalf of FSAS by Fisheries Research Services (FRS) Marine Laboratory, Aberdeen and the method used for this testing is the mouse bio-assay.

  In England and Wales similar testing is carried out by CEFAS, Weymouth and in Northern Ireland by DARD.

LIMITATIONS OF EXISTING TOXIN TESTING REGIME

  Despite the fact that the FSA was set up by the Government to inform and protect the consumer FSAS have made it very clear that it is the shellfish industry's responsibility to carry out end product testing to ensure the safety of shellfish placed on the market. FSAS therefore are only prepared to carry out sufficient toxin testing of shellfish to meet their statutory obligations to satisfy the requirements of EC Directive 492. As a tool to protect the consumer the programme is totally inadequate for three principal reasons:

  1.  FSAS will only guarantee to have test results available within seven working days of receiving the samples. As the bulk of live shellfish are harvested and placed upon the market in as little as two working days and therefore normally in the hands of the consumer within three working days the above timescale is totally inadequate.

  2.  The Standard Operating Procedure (SOP) for carrying out the mouse bio-assay has recently been changed at the insistence of FSA. The new procedure is fundamentally flawed and the results of the new bio-assay inaccurate and unreliable.

  3.  FSA accept no responsibility for ensuring that all pre-arranged samples under the programme are in fact taken and tested. If FSA have a statutory responsibility to carry out a toxin monitoring programme then surely they also have a statutory responsibility to ensure that it is carried out correctly.

  Examples of current shortfalls in the toxin testing regime are as follows:

  (a)   Late reporting

  On Tuesday, 6 May 2003 a sample of mussels was taken from Selivoe Shellfish Mussel Farm in Seli Voe, Shetland Islands and sent to the Marine Laboratory, Aberdeen on behalf of Food Standards Agency Scotland to be tested for shellfish toxins. On Friday, 9 May it was confirmed at the Marine Laboratory that the sample had tested positive for Diarrhetic Shellfish Poisoning (DSP).

  At 15.45 hrs on Friday, 9 May Marine Laboratory, Aberdeen informed Food Standards Agency Scotland of the positive DSP test.

  At 16.45 hrs on Friday May Food Standards Agency Scotland sent a fax to Environmental Services, Shetland Islands Council informing them of the test result and issuing a Voluntary Closure Order for the harvesting of mussels in Gruting/Seli Voe. This fax was sent at 16.45 hrs despite the fact that the office of Environmental Services, Shetland Islands Council closes at 16.00 hrs on a Friday.

  The fax from Food Standards Agency Scotland lay unnoticed in Shetland Islands Council offices until Tuesday, 13 May and no action was taken by Environmental Services, Shetland Islands Council until Wednesday, 14 May when the mussel farms in Gruting/Seli Voe were informed of the Voluntary Closure Order.

  On Wednesday, 14 May, five days after the positive result of the DSP test was known, A & C Tait Mussel Farm in Gruting Voe was informed of the Voluntary Closure Order by Environmental Services, Shetland Islands Council. Scottish Shellfish Marketing Group Ltd, for whom the farm was harvesting mussels, were also informed of the Voluntary Closure Order by both Environmental Services, Shetland Islands Council and the Environmental Services Department of North Lanarkshire Council on Wednesday, 14 May.

  Scottish Shellfish Marketing Group Ltd were ordered by Environmental Services Department of North Lanarkshire Council to withdraw from sale and destroy any product containing mussels harvested at A & C Tait Mussel Farm from Tuesday 6th May to Wednesday, 14 May.

  Under the toxin monitoring programme prior to the involvement of the Food Standards Agency the Marine Laboratory, Aberdeen informed directly Environmental Health Officers, affected farmers and the Scottish Executive in Pentland House, Edinburgh immediately a positive toxin test was found.

  Food Standards Agency Scotland however insisted that they would notify the Environmental Health Department responsible for the area in which the farm was located and the EHO would in turn advise the farm.

  Scottish Shellfish Marketing Group Ltd (SSMG) had made representations to both Marine Laboratory, Aberdeen and Food Standards Agency Scotland for the Marine Laboratory to contact direct both the farm and SSMG immediately a positive shellfish toxin test was known. That request was refused by Food Standards Agency Scotland. SSMG advised Food Standards Agency Scotland that their complicated method of notification could lead to delays and increase the possibility of contaminated product reaching the consumer. SSMG's advice was ignored by Food Standards Agency Scotland.

  Consumers could have been put at risk by consuming contaminated shellfish. Fortunately extensive chemical end product standard testing carried out by SSMG proved conclusively that all live mussels and processed product containing mussels harvested at A & C Tait Mussel Farm were completely free of DSP. This is not surprising as the farm sampled was in excess of three miles distant and in a separate voe from the A & C Tait Mussel Farm. The chemical end product standard testing carried out by SSMG was done at Integrin Advanced Biosystems.

  (b)   Flawed Mouse Bio-assay

  For several years the FRS Marine Laboratory, Aberdeen has carried out the statutory monitoring programme for toxins in shellfish using the Mouse Bioassay. The laboratory has refined and improved the methodology for this test over several years and the results from this test have provided safe and reliable information to the seafood industry. Industry has come to rely on this testing in conjunction with its own chemical end product standard testing to ensure that only safe and wholesome product is offered to the consumer.

  Recently two other Government Laboratories, CEFAS in Weymouth and DARD in Northern Ireland, changed the methodology they used for the Mouse Bioassay. The result of that change was that atypical positive results (false positives) were produced principally from cockles with excessive numbers of live mice being used and shellfish grounds closed for no good reason.

  The Food Standards Agency insisted that FRS, Aberdeen used the new method. FRS found, as in Weymouth and Northern Ireland, that false positive results were obtained and, on advice from the Home Office, they stopped using the new methodology and reverted to the tried and tested method.

  FSA cannot explain the reason for the false positive results and all the experienced staff in FRS, Aberdeen are convinced that the new methodology is fundamentally flawed. Despite this Food Standards Agency were determined for some perverse reason to make the new method mandatory in all UK laboratories which they did with effect from Thursday, 13 November 2003.

  This could have serious consequences for the United Kingdom in general and Scotland in particular as shellfish grounds throughout Scotland and the rest of the United Kingdom would be closed for no good reason. This would threaten the viability of a growing and vital industry to Scotland's rural communities and put an established and prosperous industry at risk in coastal areas of England and Wales.

  Since the new SOP was introduced at FRS, Aberdeen we have had three false positive results as follows:
Test dateFarm SiteFRS Mouse Bioassay Integrin Chemical
14/11/03M16Busta Voe PositiveNegative
14/11/03M15Loch Leurbost PositiveNegative
28/11/03O7Seil Sound PositiveNegative



  We understand that FRS also carried out chemical tests on these shellfish but the fact that they are not prepared to release the results of those tests is yet another example of FSA's refusal to work in harmony with industry.

  (c)   Responsibility for samples

  In August/September 2001 one of our farms based in Sutherland despatched mussels to the factory in Bellshill which we in turn sent out to wholesale customers throughout the UK. A number of food poisoning incidents occurred in various parts of the UK affecting consumers who had eaten the mussels. We discovered that a sample of mussels from the farm in question was lying in The Marine Laboratory in Aberdeen having been sent there for testing for E coli for water classification purposes. This sample was tested at our request for toxins and tested positive for DSP.

  The previous DSP test on mussels sent by the farm to the Marine Laboratory had been carried out a month earlier and had tested negative. Under the official shellfish toxin monitoring programme, which is the responsibility of Food Standards Agency Scotland, a sample should have been sent to the Marine laboratory for testing two weeks later but no sample had been sent. Despite the fact that the FSAS is responsible for the monitoring programme they claimed that it was the responsibility of the farm, not the Agency, to send in the sample.

  In light of this incident SSMG decided that it was necessary to set up our own testing regime, in addition to the official monitoring programme, to make the overall testing regime more robust and effective.

THE WAY FORWARD

  It is critical for all concerned, the shellfish industry, the Government (FSA) and the consumer to have in place a robust, comprehensive, accurate and fast reporting toxin monitoring regime that quickly identifies problems and prevents contaminated product being placed on the market. It is in no-one's interest, particularly the industry, to make people ill and lose the confidence of the consumer in healthy products that are daily growing in popularity with today's knowledgeable Public.

  It is frankly unacceptable for the FSA to shun cooperation with industry, to promote outdated and inaccurate testing methods and to accept that seven days is a reasonable timescale in which to report results thereby potentially putting the consumer at risk.

  It is time that FSA worked with and not against industry to protect the consumer and pool its resources together with those of industry to set up a testing regime based on modern mutually agreed chemical methods that reports results quickly and accurately.

Philip A Marshall

Vice Chairman

6 January 2004





 
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