Kommisjonens gjennomføringsforordning (EU) 2024/1189 av 24. april 2024 om fornyelse av godkjenningen av et preparat av Lactiplantibacillus plantarum LMG P-21295 som et tilsetningsstoff i fôr til alle dyrearter og endring av gjennomføringsforordning (EU) nr. 1065/2012
Fornyet godkjenning av Lactiplantibacillus plantarum som tilsetningsstoff i fôr til alle dyrearter
Kommisjonsforordning publisert i EU-tidende 25.4.2024
Nærmere omtale
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 renewing such authorisation.
(2) The preparation of Lactiplantibacillus plantarum (previously identified as Lactobacillus plantarum) LMG P-21295 was authorised for a period of 10 years as a feed additive for all animal species by Commission Implementing Regulation (EU) No 1065/2012 (2).
(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 Lactiplantibacillus plantarum LMG P-21295 as a feed additive for all animal species, requesting the additive to be classified in the additive category ‘technological additives’ and in the functional group ‘silage additives’. 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 27 September 2023 (3) that the preparation of Lactiplantibacillus plantarum LMG P-21295 remains safe for all animal species, the consumers and the environment under the conditions of use currently authorised. No conclusions could be drawn on the skin and eye irritation potential of the additive nor on its potential to cause skin sensitisation, but the additive should be considered a respiratory sensitiser. The Authority also indicated that there is no need for assessing the efficacy of the additive as 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 additive.
(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 Lactiplantibacillus plantarum LMG P-21295 as a feed additive in the context of the previous authorisation are valid and applicable for the current application. In accordance with Article 5(4), point (c), of Commission Regulation (EC) No 378/2005 (4), an evaluation report of the Reference Laboratory is therefore not required.
(6) In view of the above, the Commission considers that the preparation of Lactiplantibacillus plantarum LMG P-21295 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 Lactiplantibacillus plantarum LMG P-21295 as a feed additive, Implementing Regulation (EU) No 1065/2012 should be amended accordingly.
(8) Since safety reasons do not require the immediate application of the modifications to the conditions of authorisation of Lactiplantibacillus plantarum LMG P-21295, it is appropriate to provide for a transitional period for interested parties to prepare themselves to meet the new requirements resulting from the renewal of the authorisation.
(9) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,