Kommisjonens gjennomføringsforordning (EU) 2026/538 av 11. mars 2026 om godkjenning av xantangummi framstilt med Xanthomonas campestris ATCC SD 7012 eller DSM 23730 eller CNCM I-4861 eller CIP 74.23 som tilsetningsstoff i fôr til alle dyrearter unntatt katter, hunder og akvatiske arter
Godkjenning av xantangummi som tilsetningsstoff i fôr til alle dyrearter unntatt katter, hunder og akvatiske arter
Kommisjonsforordning publisert i EU-tidende 12.3.2026
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 such an authorisation. Article 10(2) of that Regulation provides for the re-evaluation of additives authorised pursuant to Council Directive 70/524/EEC (2).
(2) Xanthan gum was authorised without a time limit in accordance with Directive 70/524/EEC as a feed additive for all animal species in the group ‘emulsifying and stabilizing agents, thickeners and gelling agents’. That substance was subsequently entered in the Register of feed additives as an existing product, in accordance with Article 10(1), point (b), of Regulation (EC) No 1831/2003.
(3) In accordance with Article 10(2) of Regulation (EC) No 1831/2003 in conjunction with Article 7 thereof, an application was submitted for the re-evaluation of xanthan gum as a feed additive for all animal species. The applicant requested the additive to be classified in the additive category ‘technological additives’ and in the functional groups ‘stabilisers’ and ‘thickeners’. The application was accompanied by the particulars and documents required under Article 7(3) of Regulation (EC) No 1831/2003. By letter of 27 January 2023, the applicant withdrew the application for the re-evaluation as regards the use of xanthan gum for cats and aquatic species.
(4) The European Food Safety Authority (‘the Authority’) concluded in its opinion of 6 May 2025 (3), which revised its opinion of 24 June 2021 (4), that xanthan gum produced with Xanthomonas campestris ATCC SD 7012 or DSM 23730 or CNCM I-4861 or CIP 74.23 is safe for all animal species, other than cats and aquatic species, at certain maximum use levels according to the different target species concerned and that it is safe for the consumers and the environment. The Authority also concluded that xanthan gum produced with Xanthomonas campestris ATCC SD 7012 or DSM 23730 or CNCM I-4861 or CIP 74.23 is not irritant to the skin and is not a skin sensitiser but it could not reach any conclusions on its potential to be an eye irritant. The Authority further concluded that xanthan gum produced with Xanthomonas campestris ATCC SD 7012 or DSM 23730 or CNCM I-4861 or CIP 74.23 is an efficacious stabiliser and thickener in feedingstuffs under the proposed conditions of use. The Authority also verified the report on the method of analysis of the feed additive in feed submitted by the Reference Laboratory set up by Regulation (EC) No 1831/2003.
(5) The Commission offered the applicant, at its request, the possibility to submit supplementary data concerning the safety of use of xanthan gum produced with Xanthomonas campestris ATCC SD 7012 or DSM 23730 or CNCM I-4861 or CIP 74.23 for dogs, at a maximum level higher than the level set out in the Authority’s opinion of 6 May 2025. The use of xanthan gum produced with Xanthomonas campestris ATCC SD 7012 or DSM 23730 or CNCM I-4861 or CIP 74.23 as a feed additive for dogs will therefore be the subject of new opinion of the Authority on the basis of the supplementary data to be received, which will be considered in view of the adoption of a separate measure concerning its authorisation.
(6) In view of the above, the Commission considers that xanthan gum produced with Xanthomonas campestris ATCC SD 7012 or DSM 23730 or CNCM I-4861 or CIP 74.23 satisfies the conditions provided for in Article 5 of Regulation (EC) No 1831/2003. Accordingly, the use of that substance should be authorised for all animal species other than cats, dogs and aquatic species. In addition, the Commission considers that appropriate protective measures should be taken to prevent adverse effects on the health of the users of the additive.
(7) Since safety reasons do not require the immediate application of the modifications to the conditions of authorisation of the substance concerned, it is appropriate to provide for a transitional period for interested parties to prepare themselves to meet the new requirements resulting from the authorisation.
(8) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,