Commission Implementing Decision 2014/907/EU

law://eu/dec/2014/907@2026-11-13

Contents

THE EUROPEAN COMMISSION,Having regard to the Treaty on the Functioning of the European Union,Having regard to Regulation (EC) No 258/97 of the European Parliament and of the Council of 27 January 1997 concerning novel foods and novel food ingredients^note, and in particular Article 7 thereof,Whereas:

(1)On 2 February 2012, the company Miyarisan Pharmaceutical Co. Ltd made a request to the competent authorities of the United Kingdom to place Clostridium butyricum (CBM 588) on the market as a novel food ingredient to be used in food supplements.

(2)On 14 May 2013, the competent food assessment body of the United Kingdom issued its initial assessment report. In that report it came to the conclusion that Clostridium butyricum (CBM 588) meets the criteria for novel food set out in Article 3(1) of Regulation (EC) No 258/97.

(3)On 4 September 2013, the Commission forwarded the initial assessment report to the other Member States.

(4)Reasoned objections were raised within the 60-day period laid down in the first subparagraph of Article 6(4) of Regulation (EC) No 258/97. In accordance with Article 7(1) of Regulation (EC) No 258/97 a Commission Implementing Decision should be made that takes into account the objections raised. The additional explanations provided by the applicant alleviated the concerns to the satisfaction of the Member States and the Commission.

(5)Directive 2002/46/EC of the European Parliament and of the Council^note lays down requirements on food supplements. The use of Clostridium butyricum (CBM 588) should be authorised without prejudice to the requirements of that legislation.

(6)The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,

HAS ADOPTED THIS DECISION:

Article 1 #

Clostridium butyricum (CBM 588) as specified in the Annex may be placed on the market in the Union as a novel food ingredient to be used in food supplements with a maximum dose of 1,35 × 10⁸ CFU per day without prejudice to the specific provisions of Directive 2002/46/EC.

Total viable aerobic count	Not more than 10³ CFU/g
Escherichia coli	Not detected in 1 g
Staphylococcus aureus	Not detected in 1 g
Pseudomonas aeruginosa	Not detected in 1 g
Yeast and moulds	Not more than 10² CFU/g

Commission Implementing Decision 2014/907/EU

Commission Implementing Decision 2014/907/EU

Article 1 #

Article 2 #

Article 3 #

Specification of clostridium butyricum (cbm 588)

Microbiological criteria:

Key facts

History · 2 versions

Article 1 #

Article 2 #

Article 3 #

Specification of clostridium butyricum (cbm 588)

Microbiological criteria:

Connections