Kommisjonens gjennomføringsforordning (EU) 2026/1712 av 20. juli 2026 om endring og retting av gjennomføringsforordning (EU) 2020/1097 med hensyn til vilkårene for godkjenning av luteinrike og lutein-/zeaksantin-ekstrakter fra Tagetes erecta som fôrtilsetningsstoffer for fjørfe (unntatt kalkuner) til oppfôring og egglegging og for mindre fjørfearter til oppfôring og egglegging, og om endring av gjennomføringsforordning (EU) 2025/1928 med hensyn til vilkårene for godkjenning av luteinrikt ekstrakt av Tagetes erecta L. til oppfôringskalkuner
Godkjenning av luteinrik og lutein/zeaksantin-ekstrakt fra Tagetes erecta som tilsetningsstoff i fôrvarer til visse fjørfe
Kommisjonsforordning publisert i EU-tidende 21.7.2026
Bakgrunn
(fra kommisjonsforordningen)
(1) Regulation (EC) No 1831/2003 provides for the authorisation of additives for use in animal nutrition and for the grounds and procedures for granting and modifying such authorisation.
(2) Lutein-rich and lutein/zeaxanthin extracts from Tagetes erecta were authorised for 10 years as feed additives for poultry (except turkeys) for fattening and laying and for minor poultry species for fattening and laying by Commission Implementing Regulation (EU) 2020/1097 (2). In addition, a preparation of lutein-rich extract of Tagetes erecta L. was authorised for 10 years as a feed additive for turkeys for fattening by Commission Implementing Regulation (EU) 2025/1928 (3).
(3) In the context of the submission of the application for the authorisation of a new use of the additive lutein-rich extract from Tagetes erecta in feed for turkeys for fattening in accordance with Article 7 of Regulation (EC) No 1831/2003, the European Food Safety Authority (‘the Authority’) considered in its opinion of 18 September 2024 (4) that the manufacturing process and the composition of the additive were not substantially changed in comparison with the lutein-rich extract as authorised by Implementing Regulation (EU) 2020/1097. The first part of the manufacturing process, which is similar to that used for the production of lutein/zeaxanthin extract, as mentioned in the Authority’s opinion of 3 April 2019 (5), is the extraction with hexane of the dried flower petals of Tagetes erecta. In its opinion of 18 September 2024 regarding the specifications of the additive lutein-rich extract, the Authority recommended that the presence of hexane in the additive should be below the International Cooperation on Harmonization of Technical Requirements for Registration of Veterinary Medicinal Products (VICH) Guideline limit of 290 mg/kg. The Authority, in its plenary meeting of the Panel on Additives and Products or Substances used in Animal Feed (‘FEEDAP’) of 24-26 June 2025 (6), stated that the same recommendation would also apply to the lutein/zeaxanthin extract currently authorised in the Union.
(4) In order to ensure that the additives lutein-rich and lutein/zeaxanthin extracts from Tagetes erecta still meet the conditions provided for in Article 5 of Regulation (EC) No 1831/2003, the specification regarding the limit of 290 mg/kg of hexane in those additives should be reflected in the respective authorisations granted by Implementing Regulation (EU) 2020/1097, and hexane should be mentioned as solvent used in the extraction during the manufacturing process. Implementing Regulation (EU) 2020/1097 should therefore be amended accordingly.
(5) Implementing Regulation (EU) 2020/1097 also provides that the additives lutein-rich extract and lutein/zeaxanthin extract of Tagetes erecta must be placed on the market and used as additives consisting of a preparation, but the composition of such preparations has erroneously not been specified in the terms of the authorisation. A more accurate description of the additives authorised as preparations by Implementing Regulation (EU) 2020/1097 should be provided for, by specifying that the composition of the additives includes a total carotenoid content equal to or above 0,5 %, as specified in the Authority’ opinion of 3 April 2019. It is also appropriate to indicate the possible forms of the preparations, which may be liquid or solid, instead of the form of the active substance. Implementing Regulation (EU) 2020/1097 should therefore be corrected accordingly.
(6) Implementing Regulation (EU) 2020/1097 also provides that the mixture of the additives lutein-rich extract and lutein/zeaxanthin extract of Tagetes erecta with other authorised carotenoids and xanthophylls should not exceed the maximum content set for the corresponding animal categories. That provision should not refer to xanthophylls, in accordance with the recommendation in the Authority’s opinion of 3 April 2019, since xanthophylls are a subgroup of carotenoids. Implementing Regulation (EU) 2020/1097 should therefore be corrected accordingly.
(7) Implementing Regulation (EU) 2020/1097 was corrected by Implementing Regulation (EU) 2021/420 as regards certain provisions thereof. The end of the period of authorisation was changed in error to 30 September 2031, whereas it should not have been modified. Implementing Regulation (EU) 2020/1097 should therefore be corrected accordingly.
(8) The authorisation of the additive lutein-rich extract of Tagetes erecta by Implementing Regulation (EU) 2020/1097 and by Implementing Regulation (EU) 2025/1928 provides for similar terms of authorisation of that additive and should therefore include the same identification number. Implementing Regulation (EU) 2025/1928 should therefore be amended accordingly.
(9) On 15 January 2025, the Reference Laboratory set up by Regulation (EC) No 1831/2003 updated the report on the methods of analysis of lutein. The new method also applies to lutein-rich and lutein/zeaxanthin extracts from Tagetes erecta as authorised by Implementing Regulation (EU) 2020/1097. Implementing Regulation (EU) 2020/1097 should therefore be amended accordingly.
(10) Since safety reasons do not require the immediate application of the modifications to the conditions of authorisation of lutein-rich and lutein/zeaxanthin extracts from Tagetes erecta, it is appropriate to provide for a transitional period for interested parties to prepare themselves to meet the new requirements resulting from those modifications.
(11) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,