Kommisjonsforordning (EU) 2024/345 av 22. januar 2024 om endring av vedlegg II, III og V til europaparlaments- og rådsforordning (EF) nr. 396/2005 med hensyn til øvre grenseverdier for rester av desmedifam, etridiazol, flurtamon, profoksydim, difenacoum og kaliumpermanganat i eller på visse produkter
Øvre grenseverdier for rester av plantevernmidler i næringsmidler: endringsbestemmelser om desmedifam, etridiazol, flurtamon, profoksydim, difenacoum og kaliumpermanganat
Kommisjonsforordning publisert i EU-tidende 23.1.2024
Tidligere
- Utkast til kommisjonsforordning sendt til Europaparlamentet og Rådet for klarering og publisert i EUs komitologiregister 25.10.2023
Nærmere omtale
BAKGRUNN (fra kommisjonsforordningen)
(1) For the active substances desmedipham, flurtamone and profoxydim, maximum residue levels (‘MRLs’) were set in Annex II to Regulation (EC) No 396/2005. For the active substance etridiazole, MRLs were set in Part A of Annex III to Regulation (EC) No 396/2005. For the active substances difenacoum and potassium permanganate, no specific MRLs were set in Regulation (EC) No 396/2005, and as these active substances are not included in Annex IV to that Regulation, the default value of 0,01 mg/kg laid down in Article 18(1), point (b), of that Regulation applies.
(2) The approval of the active substance desmedipham expired on 1 July 2019 and was non-renewed. All authorisations for plant protection products containing that active substance have been revoked. No Codex maximum residue limits (‘CXLs’) or import tolerances exist for that substance. The MRLs for desmedipham on all products are set at the limit of determination (‘LOD’). In line with technical progress, lower levels of LODs are now achievable. It is therefore appropriate to lower the MRLs set out for desmedipham in Annex II to Regulation (EC) No 396/2005 to the current product specific LODs in accordance with Article 17 of Regulation (EC) No 396/2005 in conjunction with Article 14(1), point (a), thereof, and move them to Annex V to Regulation (EC) No 396/2005 in accordance with Article 18(1), point (b), of that Regulation. Additionally, as the MRLs on all products are set at the product specific LODs, there is no longer a need for confirmatory data. Therefore, all footnotes containing requests for confirmatory data should be deleted.
(3) The approval of the active substance etridiazole expired on 31 May 2021 and no application for renewal of its approval had been submitted. All authorisations for plant protection products containing that active substance have been revoked. No CXLs or import tolerances exist for that substance. It is therefore appropriate to delete the MRLs set for this substance in Part A to Annex III to Regulation (EC) No 396/2005 in accordance with Article 17 of Regulation (EC) No 396/2005 in conjunction with Article 14(1), point (a), thereof. MRLs for etridiazole on all products should be set at the product specific LODs in Annex V to Regulation (EC) No 396/2005 in accordance with Article 18(1), point (b), of that Regulation.
(4) The approval of the active substance flurtamone expired on 27 December 2018 and was non-renewed. All authorisations for plant protection products containing that active substance have been revoked. No CXLs or import tolerances exist for that substance. The MRLs for flurtamone on all products are set at the product specific LODs. It is therefore appropriate to move the MRLs set for flurtamone in Annex II to Regulation (EC) No 396/2005 to Annex V to Regulation (EC) No 396/2005 in accordance with Article 18(1), point (b), of that Regulation.
(5) The approval of the active substance profoxydim expired on 31 July 2021 and no application for renewal of its approval had been submitted. All authorisations for plant protection products containing that active substance have been revoked. No CXLs or import tolerances exist for that substance. The MRLs for profoxydim on all products are set at the product specific LODs. It is therefore appropriate to move the MRLs set for profoxydim in Annex II to Regulation (EC) No 396/2005 to Annex V to Regulation (EC) No 396/2005 in accordance with Article 18(1), point (b), of that Regulation.
(6) The approval of the active substance difenacoum expired on 30 December 2019 and no application for renewal of its approval had been submitted. All authorisations for plant protection products containing that active substance have been revoked. No CXLs or import tolerances exist for that substance. It is therefore appropriate to set the MRLs for difenacoum on all products at the product specific LODs in Annex V to Regulation (EC) No 396/2005 in accordance with Article 18(1), point (b), of that Regulation.
(7) The active substance potassium permanganate is not approved. No CXLs or import tolerances exist for that substance. It is therefore appropriate to set the MRLs for potassium permanganate on all products at the product specific LODs in Annex V to Regulation (EC) No 396/2005 in accordance with Article 18(1), point (b), of that Regulation.
(8) The Commission consulted the European Union reference laboratories for residues of pesticides as regards the need to adapt certain LODs. Those laboratories proposed product specific LODs that are analytically achievable.
(9) Through the World Trade Organisation, the trading partners of the Union were consulted on the new MRLs and their comments have been taken into account.
(10) Annexes II, III and V to Regulation (EC) No 396/2005 should therefore be amended accordingly.
(11) To allow for the normal marketing, processing and consumption of products, this Regulation should not apply to products, which have been produced in the Union or imported into the Union before the new MRLs become applicable and for which a high level of consumer protection is maintained.
(12) A reasonable period should be allowed to elapse before the new MRLs become applicable in order to permit Member States, third countries and food business operators to adapt themselves to the requirements which result from the modification of the MRLs.
(13) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,