PDF《REGULATIONS》

II (Non-legislative acts) REGULATIONS COMMISSION REGULATION (EU) No 310/2011 of

28 March

2011 amending Annexes II and III to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for aldicarb, bromopropylate, chlorfenvinphos, endosulfan, EPTC, ethion, fenthion, fomesafen, methabenzthiazuron, methidathion, simazine, tetradifon and triforine in or on certain products (Text with EEA relevance) THE EUROPEAN COMMISSION, Having regard to the Treaty on the Functioning of the European Union, Having regard to Regulation (EC) No 396/2005 of the European Parliament and of the Council of

23 February

2005 on maximum residue levels of pesticides in or on food and feed of plant and animal origin and amending Council Directive 91/414/EEC (1), and in particular Article 14(1)(a) thereof, Whereas: (1) For aldicarb, bromopropylate, chlorfenvinphos, endo? sulfan, EPTC, ethion, fenthion, methidathion, simazine and triforine maximum residue levels (MRLs) are set in Annex II and Part B of Annex III to Regulation (EC) No 396/2005.

For fomesafen, methabenzthiazuron and tetradifon MRLs were set in Part A of Annex III to Regulation (EC) No 396/2005. (2) The non-inclusion of aldicarb in Annex I to Council Directive 91/414/EEC (2) is provided for in Council Decision 2003/199/EC (3) and certain Member States were authorised to grant a period of grace expiring no later than

31 December 2007. The non-inclusion of bromopropylate, chlorfenvinphos, EPTC, ethion, fomesafen, tetradifon and triforine is provided for in Commission Regulation (EC) No 2076/2002 (4) and certain Member States were authorised to grant a period of grace expiring no later than

31 December 2007. The non-inclusion of endosulfan in Annex I to Directive 91/414/EEC is provided for in Commission Decision 2005/864/EC (5) and certain Member States were au- thorised to grant a period of grace expiring no later than

31 December 2007. The non-inclusion of fenthion in Annex I to Directive 91/414/EEC is provided for in Commission Decision 2004/140/EC (6) and certain Member States were authorised to grant a period of grace expiring no later than

31 December 2007. The non-inclusion of methabenzthiazuron in Annex I to Directive 91/414/EEC is provided for in Commission Decision 2006/302/EC (7) and certain Member States were authorised to grant a period of grace expiring no later than

31 December 2009. The non-inclusion of methidathion in Annex I to Directive 91/414/EEC is provided for in Commission Decision 2004/129/EC (8) and certain Member States were auth? orised to grant a period of grace expiring no later than

31 December 2007.The non-inclusion of simazine in Annex I to Directive 91/414/EEC is provided for in Commission Decision 2004/247/EC (9) and certain Member States were authorised to grant a period of grace expiring no later than

31 December 2007. (3) Since those periods of grace have expired, it is appro? priate to lower the MRLs of those substances to the relevant level of analytical determination (LOD). This should not apply to CXLs based on uses in third countries, provided that those CXLs are acceptable with regard to consumer safety. Nor should it apply in cases where MRLs have been specifically set as import tolerances. EN 1.4.2011 Official Journal of the European Union L 86/1 (1) OJ L 70, 16.3.2005, p. 1. (2) OJ L 230, 19.8.1991, p. 1. (3) OJ L 76, 22.3.2003, p. 21. (4) OJ L 319, 23.11.2002, p. 3. (5) OJ L 317, 3.12.2005, p. 25. (6) OJ L 46, 17.2.2004, p. 32. (7) OJ L 112, 26.4.2006, p. 15. (8) OJ L 37, 10.2.2004, p. 27. (9) OJ L 78, 16.3.2004, p. 50. (4) The Commission asked the European Food Safety Authority, hereinafter '