Commission Implementing Regulation (EU) 2021/1318 of 9 August 2021 correcting Implementing Regulation (EU) 2017/2470 establishing the Union list of novel foods, Decision 2008/968/EC authorising the placing on the market of arachidonic acid-rich oil from Mortierella alpina as a novel food ingredient and Implementing Regulation (EU) 2020/484 authorising the placing on the market of lacto-N-tetraose as a novel food (Text with EEA relevance)

Type Implementing Regulation
Publication 2021-08-10
State In force
Text As published
Department European Commission, SANTE
Source EUR-Lex
articles 4

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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10.8.2021 EN Official Journal of the European Union L 286/5

THE EUROPEAN COMMISSION,

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

Having regard to Regulation (EU) 2015/2283 of the European Parliament and of the Council of 25 November 2015 on novel foods, amending Regulation (EU) No 1169/2011 of the European Parliament and of the Council and repealing Regulation (EC) No 258/97 of the European Parliament and of the Council and Commission Regulation (EC) No 1852/2001 1, and in particular Article 12 thereof,

Whereas:

HAS ADOPTED THIS REGULATION:

Article 1

The second paragraph of Article 1 of the Decision 2008/968/EC is corrected as follows:

‘The addition of fungal oil from Mortierella alpina to infant formulae and follow-on formulae shall be limited by its content of arachidonic acid according to the rules specified in Annex I, 5.7 and in Annex II, 4.7 to Directive 2006/141/EC. Its use in formulae for infants shall be in accordance with the provisions of Council Directive 89/398/EEC(*1) on the approximation of the laws of the Member States relating to foodstuffs intended for particular nutritional uses.

Article 2

The Annex to Implementing Regulation (EU) 2020/484 is corrected in accordance with the Annex to this Regulation.

Article 3

The Annex to Implementing Regulation (EU) 2017/2470 is corrected in accordance with the Annex to this Regulation.

Article 4

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, 9 August 2021.

For the Commission

The President

Ursula VON DER LEYEN

2

Regulation (EC) No 258/97 of the European Parliament and of the Council of 27 January 1997 concerning novel foods and novel food ingredients (OJ L 43, 14.2.1997, p. 1).

3

Commission Implementing Regulation (EU) 2017/2470 of 20 December 2017 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel foods (OJ L 351, 30.12.2017, p. 72).

4

Commission Decision 2008/968/EC of 12 December 2008 authorising the placing on the market of arachidonic acid-rich oil from Mortierella alpina as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council (OJ L 344, 20.12.2008, p. 123).

5

Letter of 19 December 2011 (https://ec.europa.eu/food/system/files/2016-10/novel-food_authorisation_2011_auth-letter_arachidonic_acid_rich_oil_en.pdf).

6

https://doi.org/10.2903/j.efsa.2004.135.

7

Commission Delegated Regulation (EU) 2021/571 of 20 January 2021 amending the Annex to Regulation (EU) No 609/2013 of the European Parliament and of the Council as regards the list of substances that may be added to infant and follow-on formula, baby food and processed cereal-based food (OJ L 120, 8.4.2021, p. 1).

8

Commission Implementing Regulation (EU) 2020/484 of 2 April 2020 authorising the placing on the market of lacto-N-tetraose as a novel food under Regulation (EU) 2015/2283 of the European Parliament and of the Council and amending Commission Implementing Regulation (EU) 2017/2470 (OJ L 103, 3.4.2020, p. 3).

ANNEX

Authorised novel food Conditions under which the novel food may be used Conditions under which the novel food may be used Additional specific labelling requirements Other requirements
“Arachidonic acid-rich oil from the fungus Mortierella alpina Specified food category Maximum levels The designation of the novel food on the labelling of the foodstuffs containing it shall be ‘Oil from Mortierella alpina’ or ‘Mortierella alpina oil’”
“Arachidonic acid-rich oil from the fungus Mortierella alpina Infant formula and follow-on formula as defined in Regulation (EU) No 609/2013 In accordance with Regulation (EU) No 609/2013 The designation of the novel food on the labelling of the foodstuffs containing it shall be ‘Oil from Mortierella alpina’ or ‘Mortierella alpina oil’”
“Arachidonic acid-rich oil from the fungus Mortierella alpina Foods for special medical purposes for infants as defined in Regulation (EU) No 609/2013 In accordance with Regulation (EU) No 609/2013 The designation of the novel food on the labelling of the foodstuffs containing it shall be ‘Oil from Mortierella alpina’ or ‘Mortierella alpina oil’”
“Calcium L-Methylfolate Specified food category Maximum levels (expressed as folic acid) The designation of the novel food on the labelling of the foodstuffs containing it shall be ‘Calcium L-Methylfolate’.”
“Calcium L-Methylfolate Foods for special medical purposes and total diet replacement for weight control as defined in Regulation (EU) No 609/2013 In accordance with Regulation (EU) No 609/2013 The designation of the novel food on the labelling of the foodstuffs containing it shall be ‘Calcium L-Methylfolate’.”
“Calcium L-Methylfolate Infant formulae and follow-on formula as defined by Regulation (EU) No 609/2013 In accordance with Regulation (EU) No 609/2013 The designation of the novel food on the labelling of the foodstuffs containing it shall be ‘Calcium L-Methylfolate’.”
“Calcium L-Methylfolate Processed cereal-based foods and baby foods for infants and young children as defined by Regulation (EU) No 609/2013 In accordance with Regulation (EU) No 609/2013 The designation of the novel food on the labelling of the foodstuffs containing it shall be ‘Calcium L-Methylfolate’.”
“Calcium L-Methylfolate Food supplements as defined in Directive 2002/46/EC excluding food supplements for infants and young children In accordance with Directive 2002/46/EC The designation of the novel food on the labelling of the foodstuffs containing it shall be ‘Calcium L-Methylfolate’.”
“Calcium L-Methylfolate Food fortified in accordance with Regulation (EC) No 1925/2006 In accordance with Regulation (EU) No 1925/2006 The designation of the novel food on the labelling of the foodstuffs containing it shall be ‘Calcium L-Methylfolate’.”
“Calcium L-Methylfolate Description: The novel food is produced by chemical synthesis starting from folic acid. It is a white to light yellowish, almost odourless, crystalline powder, sparingly soluble in water and very slightly soluble or insoluble in most organic solvents. Definition: Chemical formula: C20H23CaN7O6 Systematic name: N-{4-[[((6S)-2-amino-1,4,5,6,7,8-hexahydro-5-methyl-4-oxo-6-pteridinyl)methyl]amino]benzoyl}-L-glutamic acid, calcium salt. CAS Numbers: 129025-21-4 (Calcium salt with an unspecified ratio of L-5-MTHF/Ca2+) and 151533-22-1 (Calcium salt with specified 1:1 ratio of L-5-MTHF/Ca2+). Molecular weight: 497,5 Daltons Synonyms: L-methylfolate, calcium; L-5-methyltetrahydrofolic acid, calcium salt [(L-5-MTHF-Ca)]; (6S)-5-methyltetrahydrofolic acid, calcium salt [(6S)-5-MTHF-Ca]; (6S)-5-methyl-5,6,7,8-tetrahydropteroyl-L-glutamic acid, calcium salt, and L-5-methyl-tetrahydrofolic acid (L-5-MTHF) without the cation specified. Structural formula: Image omitted; see official source Characteristics Purity: > 95 % (Dry basis) Water: ≤ 17.0 % Calcium (on anhydrous and solvent free basis): 7.0 – 8.5 % Calcium D-methylfolate (6R, αS isomer): ≤ 1.0 % Other folates and related substances: ≤ 2.5 % Ethanol: ≤ 0.5 % Lead: ≤ 1 mg/kg Boron: ≤ 10 mg/kg Cadmium ≤ 0.5 mg/kg Mercury ≤ 1.0 mg/kg Arsenic ≤ 1.5 mg/kg Platinum ≤ 2 mg/kg Microbiological criteria: Total viable aerobic counts: ≤ 1 000 CFU/g Total yeast and mould count: ≤ 100 CFU/g
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CFU :

The entry for ‘Lacto-N-tetraose (‘LNT’) (microbial source)’ in Table 2 (Specifications) is replaced by the following:

“Lacto-N-tetraose (‘LNT’) (microbial source) Definition: Chemical formula: C26H45NO21 Chemical name: β-D-Galactopyranosyl-(1→3)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→3)-β-D-galactopyranosyl-(1→4)-D-glucopyranose Molecular mass: 707.63 Da CAS No 14116-68-8 Description: Lacto-N-tetraose is a purified, white to off-white amorphous powder or agglomerates that is produced by a microbial process. Source: Genetically modified strain of Escherichia coli strain K-12 DH1 Characteristics/Composition: Appearance: White to off white powder or agglomerates Sum of lacto-N-tetraose, D-Lactose and lacto-N-triose II (% of dry matter): ≥ 90.0 % (w/w) Lacto-N-tetraose (% of dry matter): ≥ 70.0 % (w/w) D-Lactose: ≤ 12.0 % (w/w) Lacto-N-triose II: ≤ 10.0 % (w/w) Para-lacto-N-hexaose-2: ≤ 3.5 % (w/w) Lacto-N-tetraose fructose isomer: ≤ 1.0 % (w/w) Sum of other carbohydrates: ≤ 5.0 % (w/w) Moisture: ≤ 6.0 % (w/w) Ash, sulfated: ≤ 0.5 % (w/w) pH (20 °C, 5 % solution): 4.0 -6.0 Residual protein: ≤ 0.01 % (w/w) Microbiological criteria: Aerobic mesophilic bacteria total plate count: ≤ 1 000 CFU/g Enterobacteriaceae: ≤ 10 CFU/g Salmonella spp.: Negative/25 g Yeast: ≤ 100 CFU/g Mould: ≤ 100 CFU/g Residual endotoxins: ≤ 10 EU/mg
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CFU :

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