(Utkast) Kommisjonsforordning (EU) .../... om endring av vedlegg II og III til europaparlaments- og rådsforordning (EF) nr. 396/2005 med hensyn til øvre grenseverdier for rester av acekvinocyl, klormekvat, metalaksyl-M, pyraklostrobin, sulfoksaflor og trifloksystrobin i eller på visse produkter
Øvre grenseverdier for rester av plantevernmidler i næringsmidler: acekvinocyl, klormekvat, metalaksyl-M, pyraklostrobin, sulfoksaflor og trifloksystrobin
Utkast til kommisjonsforordning sendt til Europaparlamentet og Rådet for klarering og publisert i EUs komitologiregister 19.9.2025
Bakgrunn
(fra kommisjonsforordningen)
(1) For acequinocyl, metalaxyl-M, pyraclostrobin, sulfoxaflor and trifloxystrobin, maximum residue levels (‘MRLs’) were set in Annex II to Regulation (EC) No 396/2005. For the active substance chlormequat, temporary MRLs were set in Part A of Annex III to that Regulation.
(2) As regards acequinocyl, an application requesting a modification of the existing MRLs was submitted for strawberries, pursuant to Article 6(1) of Regulation (EC) No 396/2005. As regards chlormequat, such an application was submitted for oats. As regards metalaxyl-M, such an application was submitted for honey and other apiculture products. As regards pyraclostrobin, such an application was submitted for sweet corn. As regards sulfoxaflor, such an application was submitted for okra/lady's fingers, lamb’s lettuces/corn salads, escaroles/broad-leaved endives, cresses and other sprouts and shoots, land cresses, roman rocket/rucola, red mustards, baby leaf crops (including brassica species), purslanes, chard/beet leaves, watercresses, chervil, chives, parsley, sage, rosemary, thyme, basil and edible flowers, laurel/bay leaves and tarragon. As regards trifloxystrobin, such an application was submitted for table olives, olives for oil production, celeries, globe artichokes, leeks, herbal infusions from flowers, herbal infusions from leaves and herbs and seed spices.
(3) In addition, as regards trifloxystrobin in linseeds, an application for an import tolerance pursuant to Article 6(2) and (4) of Regulation (EC) No 396/2005 was submitted based on a use of that active substance in Canada.
(4) In accordance with Articles 8 and 9 of Regulation (EC) No 396/2005, all those applications were evaluated by the Member States concerned and the evaluation reports were forwarded to the Commission. The Commission forwarded the applications, the evaluation reports and the supporting dossiers to the European Food Safety Authority (‘the Authority’).
(5) The Authority assessed the applications and the evaluation reports, examining in particular the risks to consumers and, where relevant, to animals, and gave reasoned opinions on the proposed MRLs2 . It forwarded those opinions to the applicants, the Commission and Member States and made them available to the public.
(6) As regards all those applications, except trifloxystrobin in herbal infusions from flowers and in herbal infusions from leaves and herbs, the Authority concluded that the data were appropriate to derive or confirm the MRL proposals for the commodities under assessment. It is therefore appropriate to set the requested MRLs for acequinocyl in strawberries, chlormequat in oats, metalaxyl-M in honey and other apiculture products, for pyraclostrobin in sweet corn, for sulfoxaflor in okra/lady’s fingers, lamb’s lettuces/corn salads, escaroles/broad-leaved endives, cresses and other sprouts and shoots, land cresses, roman rocket/rucola, red mustards, baby leaf crops (including brassica species), purslanes, chard/beet leaves, watercresses, chervil, chives, parsley, sage, rosemary, thyme, basil and edible flowers, laurel/bay leaves and tarragon and for trifloxystrobin in table olives, olives for oil production, celeries, globe artichokes, leeks, linseeds and seed spices at the levels recommended by the Authority.
(7) As regards trifloxystrobin in herbal infusions from flowers and in herbal infusions from leaves and herbs, the Authority concluded that the risk for consumers is unlikely despite considering that two residue field trials do not fully meet the independence criteria as defined in the Technical Guidelines. In view of the fact that the two concerned residue field trials did not overlap in time and that they were conducted at different sites, a risk management decision is made to consider these trials as independent. It is considered appropriate to set the requested MRLs for trifloxystrobin in herbal infusions from flowers and in herbal infusions from leaves and herbs at the level recommended by the Authority.
(8) Regulation (EC) No 396/2005 should therefore be amended accordingly.
(9) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,