Commission Implementing Regulation (EU) 2024/859 of 18 March 2024 amending Regulation (EU) No 37/2010 as regards the classification of the substance sodium salicylate with respect to its maximum residue limit in foodstuffs of animal origin

Type Implementing Regulation
Publication 2024-03-19
State In force
Text As published
Department European Commission, SANTE
Source EUR-Lex
articles 2

This is the act as published. Later amendments are not folded into the text below: each one is a separate act in this repository and an entry in this law's history.

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Image omitted; see official source Official Journal of the European Union EN Series L
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2024/859 19.3.2024

THE EUROPEAN COMMISSION,

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

Having regard to Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council 1, and in particular Article 14, in conjunction with Article 17, thereof,

Whereas:

HAS ADOPTED THIS REGULATION:

Article 1

The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.

Article 2

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, 18 March 2024.

For the Commission

The President

Ursula VON DER LEYEN

2

Commission Regulation (EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin (OJ L 15, 20.1.2010, p. 1).

3

Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (OJ L 4, 7.1.2019, p. 43).

ANNEX

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the pharmacologically active substance ‘sodium salicylate’ is replaced by the following:

Pharmacologically active Substance Marker residue Animal Species MRL Target Tissues Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic Classification
‘Sodium salicylate NOT APPLICABLE Bovine, Porcine No MRL required NOT APPLICABLE For oral use. Not for use in animals from which milk is produced for human consumption. NO ENTRY
‘Sodium salicylate NOT APPLICABLE All food producing species except fin fish No MRL required NOT APPLICABLE For topical use only. NO ENTRY
‘Sodium salicylate Salicylic acid Turkey 400 μg/kg 2 500 μg/kg 200 μg/kg 150 μg/kg Muscle Skin and fat in natural proportions Liver Kidney Not for use in animals producing eggs for human consumption. Anti-inflammatory agents / Non-steroidal anti-inflammatory agents’.
‘Sodium salicylate Salicylic acid Poultry other than turkey 250 μg/kg 250 μg/kg 500 μg/kg 1 000 μg/kg Muscle Skin and fat in natural proportions Liver Kidney Not for use in animals producing eggs for human consumption. Anti-inflammatory agents / Non-steroidal anti-inflammatory agents’.

ELI: http://data.europa.eu/eli/reg_impl/2024/859/oj

ISSN 1977-0677 (electronic edition)

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