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Commission Implementing Regulation (EU) 2026/155 of 23 January 2026 concerning the renewal of the authorisation of a preparation of Saccharomyces cerevisiae NCYC R404 as a feed additive for cows (holder of authorisation: Volac International Ltd) and repealing Implementing Regulation (EU) 2015/502

Type Implementing Regulation

Publication 2026-01-26

State In force

Text As published

Department European Commission, SANTE

Source EUR-Lex

articles 3

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Image omitted; see official source	Official Journal of the European Union	EN L series

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	2026/155	26.1.2026

THE EUROPEAN COMMISSION,

Having regard to the Treaty on the Functioning of the European Union,

Having regard to Regulation (EC) No 1831/2003 of the European Parliament and of the Council of 22 September 2003 on additives for use in animal nutrition [^ntr1-L_202600155EN.000101-E0001], and in particular Article 9(2) thereof,

Whereas:

(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 renewing such an authorisation.

(2) A preparation of Saccharomyces cerevisiae NCYC R404, was authorised for a period of 10 years as a feed additive for dairy cows by Commission Implementing Regulation (EU) 2015/502 [^ntr2-L_202600155EN.000101-E0002].

(3) In accordance with Article 14(1) of Regulation (EC) No 1831/2003, an application was submitted for the renewal of the authorisation of the preparation of Saccharomyces cerevisiae NCYC R404 as a feed additive for dairy cows, requesting the additive to be classified in the additive category ‘zootechnical additives’ and in the functional group ‘gut flora stabilisers’. That application was accompanied by the particulars and documents required under Article 14(2) of Regulation (EC) No 1831/2003.

(4) The European Food Safety Authority (‘the Authority’) concluded in its opinion of 18 March 2025 [^ntr3-L_202600155EN.000101-E0003] that the preparation of Saccharomyces cerevisiae NCYC R404 remains safe for dairy cows, consumers and the environment under the conditions of use currently authorised. It also concluded that the preparation of Saccharomyces cerevisiae NCYC R404, is not irritant to skin or eyes, and it should be considered a potential skin and respiratory sensitiser, and any exposure through skin and respiratory tract is considered a risk. The Authority stated that the application for renewal of the authorisation does not include a proposal for amending or supplementing the conditions of the original authorisation that would have an impact on the efficacy of the additives. Therefore, it concluded that there is no need for assessing the efficacy of the additives in the context of the renewal of the authorisation. The Authority did not consider that there is a need for specific requirements of post-market monitoring.

(5) The Reference Laboratory set up by Regulation (EC) No 1831/2003 considered that the conclusions and recommendations reached in the assessment carried out regarding the method of analysis of the preparation of Saccharomyces cerevisiae NCYC R404 as a feed additive in the context of the previous authorisations are valid and applicable for the current application. In accordance with Article 5(4), point (c), of Commission Regulation (EC) No 378/2005 [^ntr4-L_202600155EN.000101-E0004], an evaluation report of the Reference Laboratory is therefore not required.

(6) In view of the above, the Commission considers that the preparation of Saccharomyces cerevisiae NCYC R404 satisfies the conditions provided for in Article 5 of Regulation (EC) No 1831/2003. Accordingly, the authorisation of that additive should be renewed. 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. Those protective measures should be without prejudice to other workers’ safety requirements under Union law.

(7) As a consequence of the renewal of the authorisation of the preparation of Saccharomyces cerevisiae NCYC R404 as a feed additive, Implementing Regulation (EU) 2015/502 should be repealed.

(8) 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

Renewal of the authorisation

The authorisation of the preparation specified in the Annex, belonging to the additive category ‘zootechnical additives’ and to the functional group ‘gut flora stabilisers’, is renewed subject to the conditions laid down in that Annex.

Article 2

Repeal

Implementing Regulation (EU) 2015/502 is repealed.

Article 3

Entry into force

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, 23 January 2026.

For the Commission

The President

Ursula VON DER LEYEN

[^ntr1-L_202600155EN.000101-E0001]: OJ L 268, 18.10.2003, p. 29, ELI: http://data.europa.eu/eli/reg/2003/1831/oj.

[^ntr2-L_202600155EN.000101-E0002]: Commission Implementing Regulation (EU) 2015/502 of 24 March 2015 concerning the authorisation of the preparation of Saccharomyces cerevisiae NCYC R404 as a feed additive for dairy cows (holder of the authorisation Micron Bio-System Ltd) (OJ L 79, 25.3.2015, p. 57, ELI: http://data.europa.eu/eli/reg_impl/2015/502/oj).

[^ntr3-L_202600155EN.000101-E0003]: EFSA Journal. 2025;23:e9342. https://doi.org/10.2903/j.efsa.2025.9342.

[^ntr4-L_202600155EN.000101-E0004]: Commission Regulation (EC) No 378/2005 of 4 March 2005 on detailed rules for the implementation of Regulation (EC) No 1831/2003 of the European Parliament and of the Council as regards the duties and tasks of the Community Reference Laboratory concerning applications for authorisations of feed additives (OJ L 59, 5.3.2005, p. 8, ELI: http://data.europa.eu/eli/reg/2005/378/oj).

ANNEX

Identification number of the feed additive	Name of the holder of authorisation	Name of the additive	Composition, chemical formula, description, analytical method	Species or category of animal	Maximum age	Minimum content	Maximum content	Other provisions	End of period of authorisation
Identification number of the feed additive	Name of the holder of authorisation	Name of the additive	Composition, chemical formula, description, analytical method	Species or category of animal	Maximum age	CFU/kg of complete feed with a moisture content of 12 %	CFU/kg of complete feed with a moisture content of 12 %	Other provisions	End of period of authorisation
Category: zootechnical additives. Functional group: gut flora stabilisers.	Category: zootechnical additives. Functional group: gut flora stabilisers.	Category: zootechnical additives. Functional group: gut flora stabilisers.	Category: zootechnical additives. Functional group: gut flora stabilisers.	Category: zootechnical additives. Functional group: gut flora stabilisers.	Category: zootechnical additives. Functional group: gut flora stabilisers.	Category: zootechnical additives. Functional group: gut flora stabilisers.	Category: zootechnical additives. Functional group: gut flora stabilisers.	Category: zootechnical additives. Functional group: gut flora stabilisers.	Category: zootechnical additives. Functional group: gut flora stabilisers.
4b1871	Volac International Ltd	Saccharomyces cerevisiae NCYC R404	Additive composition Preparation of Saccharomyces cerevisiae NCYC R404 containing a minimum of 1 × 10¹⁰ CFU/g additive Solid form Characterisation of the active substance Saccharomyces cerevisiae NCYC R404. Analytical method [^ntr1-L_202600155EN.000301-E0001] Enumeration: Pour plate method using yeast extract dextrose chloramphenicol (CGYE) agar – EN 15789 Identification: Polymerase Chain Reaction (PCR) – (CEN/TS 15790)	Cows	-	4,4 × 10⁸		1. In the directions for use of the additive and premixtures, the storage conditions and stability to heat treatment shall be indicated. 2. The additive shall be used ensuring a minimum dose of: 1 × 10¹⁰ CFU/animal/day. 3. For users of the additive and premixtures, feed business operators shall establish operational procedures and organisational measures to address potential risks resulting from their use. Where those risks cannot be eliminated by such procedures and measures, the additive and premixtures shall be used with personal breathing and skin protective equipment.	15 February 2036

[^ntr1-L_202600155EN.000301-E0001]: Details of the analytical methods are available at the following address of the Reference Laboratory: https://joint-research-centre.ec.europa.eu/eurl-fa-eurl-feed-additives/eurl-fa-authorisation/eurl-fa-evaluation-reports_en.

ELI: http://data.europa.eu/eli/reg_impl/2026/155/oj

ISSN 1977-0677 (electronic edition)

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