Commission Implementing Regulation (EU) 2022/801 of 20 May 2022 amending Implementing Regulation (EU) No 540/2011 to update the list of active substances approved or deemed to have been approved under Regulation (EC) No 1107/2009 of the European Parliament and of the Council (Text with EEA relevance)
Date: 2022-05-20
Institutions: Directorate-General for Health and Food Safety, European Commission
Subjects: market approval, plant health control, plant health product, withdrawal from the market








L_2022143EN.01000701.xml










23.5.2022   


EN


Official Journal of the European Union


L 143/7








            COMMISSION IMPLEMENTING REGULATION (EU) 2022/801
of 20 May 2022
         
amending Implementing Regulation (EU) No 540/2011 to update the list of active substances approved or deemed to have been approved under Regulation (EC) No 1107/2009 of the European Parliament and of the Council
(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 1107/2009 of the European Parliament and of the Council of 21 October 2009 concerning the placing of plant protection products on the market and repealing Council Directives 79/117/EEC and 91/414/EEC (1), and in particular Article 78(2) thereof,

Whereas:







(1)


Part A of the Annex to Commission Implementing Regulation (EU) No 540/2011 (2) lists the active substances, which were initially included in Annex I to Council Directive 91/414/EEC (3) and are deemed to have been approved under Regulation (EC) No 1107/2009. It originally listed 354 active substances.












(2)


For 68 of the active substances listed in Part A of the Annex to Implementing Regulation (EU) No 540/2011, applications for renewal were either not submitted or were submitted but withdrawn, with the consequence that the approval periods for these active substances have expired.












(3)


Part B of the Annex to Implementing Regulation (EU) No 540/2011 lists active substances approved under Regulation (EC) No 1107/2009. For 7 of those active substances, applications for renewal were either not submitted three years before the expiry of their respective approvals or were submitted but withdrawn, with the consequence that the approval periods for these active substances have expired.












(4)


All those substances that are no longer approved or deemed to have been approved following the expiry of an approval period listed for the substances concerned in either Part A or B of the Annex to Implementing Regulation (EU) No 540/2011should be deleted from the Parts A and B, respectively, of the Annex to Implementing Regulation (EU) No 540/2011 for the sake of clarity and transparency.












(5)


Implementing Regulation (EU) No 540/2011 should therefore be amended accordingly.












(6)


The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,





HAS ADOPTED THIS REGULATION:



Article 1
The Annex to Implementing Regulation (EU) No 540/2011 is amended in accordance with the Annex to this Regulation.


Article 2
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.




This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 20 May 2022.


For the Commission


The President

Ursula VON DER LEYEN
            





(1)  
            OJ L 309, 24.11.2009, p. 1.

(2)  Commission Implementing Regulation (EU) No 540/2011 of 25 May 2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the list of approved active substances (OJ L 153, 11.6.2011, p. 1).

(3)  Council Directive 91/414/EEC of 15 July 1991 concerning the placing of plant protection products on the market (OJ L 230, 19.8.1991, p. 1).




ANNEX
The Annex to Implementing Regulation (EU) No 540/2011 is amended as follows:






1.


In Part A the following entries are deleted:






(1)


entry 21, Cyclanilide;










(2)


entry 33, Cinidon-ethyl;










(3)


entry 43, Ethoxysulfuron;










(4)


entry 45, Oxadiargyl;










(5)


entry 49, Cyfluthrin;










(6)


entry 56, Mecoprop;










(7)


entry 72, Molinate;










(8)


entry 87, Ioxynil;










(9)


entry 94, Imazosulfuron;










(10)


entry 100, Tepraloxydim;










(11)


entry 113, Maneb;










(12)


entry 120, Warfarin;










(13)


entry 121, Clothianidin;










(14)


entry 140, Thiamethoxam;










(15)


entry 143, Flusilazole;










(16)


entry 144, Carbendazim;










(17)


entry 151, Glufosinate;










(18)


entry 157, Fipronil;










(19)


entry 174, Diflubenzuron;










(20)


entry 175, Imazaquin;










(21)


entry 177, Oxadiazon;










(22)


entry 184, Quinoclamine;










(23)


entry 185, Chloridazon;










(24)


entry 190, Fuberidazole;










(25)


entry 192, Diuron;










(26)


entry 196, Bacillus thuringiensis subsp. tenebrionis strain NB 176 (TM 141);










(27)


entry 201, Phlebiopsis gigantean strains VRA 1985, VRA 1986, FOC PG B20/5, FOC PG SP log 6, FOC PG SP log 5, FOC PG BU 3, FOC PG BU 4, FOC PG97/1062/116/1.1, FOC PG B22/SP1287/3.1, FOC PG SH 1, FOC PG B22/SP1190/3.2;










(28)


entry 205, Trichoderma polysporum strain IMI 206039;










(29)


entry 211, Epoxiconazole;










(30)


entry 212, Fenpropimorph;










(31)


entry 214, Tralkoxydim;










(32)


entry 216, Imidacloprid;










(33)


entry 221, Ammonium acetate;










(34)


entry 226, Denathonium benzoate;










(35)


entry 237, Limestone;










(36)


entry 239, Pepper dust extraction residue (PDER);










(37)


entry 245, 1,4-diaminobutane (putrescine);










(38)


entry 252, Sea-algae extract (formerly sea algae extract and sea weeds);










(39)


entry 253, Sodium aluminium silicate;










(40)


entry 254, Sodium hypochlorite;










(41)


entry 256, Trimethylamine hydrochloride;










(42)


entry 261, Calcium phosphide;










(43)


entry 269, Triadimenol;










(44)


entry 270, Methomyl;










(45)


entry 280, Teflubenzuron;










(46)


entry 281, Zeta-cypermethrin;










(47)


entry 282, Chlorsulfuron;










(48)


entry 283, Cyromazine;










(49)


entry 286, Lufenuron;










(50)


entry 290, Difenacoum;










(51)


entry 303, Spirodiclofen;










(52)


entry 306, Triflumizole;










(53)


entry 308, FEN 560 (also called fenugreek or fenugreek seed powder);










(54)


entry 309, Haloxyfop-P;










(55)


entry 312, Metosulam;










(56)


entry 315, Fenbuconazole;










(57)


entry 319, Myclobutanil;










(58)


entry 321, Triflumuron;










(59)


entry 324, Diethofencarb;










(60)


entry 325, Etridiazole;










(61)


entry 327, Oryzalin;










(62)


entry 332, Fenoxycarb;










(63)


entry 336, Carbetamide;










(64)


entry 337, Carboxin;










(65)


entry 338, Cyproconazole;










(66)


entry 347, Bromadiolone;










(67)


entry 349, Pencycuron;










(68)


entry 353, Flutriafol.














2.


In Part B the following entries are deleted:






(1)


entry 2, Profoxydim;










(2)


entry 3, Azimsulfuron;










(3)


entry 14, Fluquinconazole;










(4)


entry 17, Triazoxide;










(5)


entry 19, Acrinathrin;










(6)


entry 20, Prochloraz;










(7)


entry 23, Bifenthrin.