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Scientific opinion on the renewal of the authorisation of Zesti Smoke Code 10 (SF‐002) as a smoke flavouring Primary Product

Authors :
EFSA Panel name on Food Additives and Flavourings (FAF)
Maged Younes
Gabriele Aquilina
Laurence Castle
Gisela Degen
Karl‐Heinz Engel
Paul J Fowler
Maria Jose Frutos Fernandez
Peter Fürst
Ursula Gundert‐Remy
Rainer Gürtler
Trine Husøy
Melania Manco
Peter Moldeus
Sabina Passamonti
Romina Shah
Ine Waalkens‐Berendsen
Matthew Wright
Romualdo Benigni
Polly Boon
Claudia Bolognesi
Eugenia Cordelli
Kevin Chipman
Ullrika Sahlin
Maria Carfì
Carla Martino
Salvatore Multari
Vasantha Palaniappan
Alexandra Tard
Wim Mennes
Source :
EFSA Journal, Vol 21, Iss 11, Pp n/a-n/a (2023)
Publication Year :
2023
Publisher :
Wiley, 2023.

Abstract

Abstract The EFSA Panel on Food Additives and Flavourings (FAF) was requested to evaluate the safety of the smoke flavouring Primary Product Zesti Smoke Code 10 (SF‐002), for which a renewal application was submitted in accordance with Article 12(1) of Regulation (EC) No 2065/2003. This opinion refers to the assessment of data submitted on chemical characterisation, dietary exposure and genotoxicity of the Primary Product. Zesti Smoke Code 10 is obtained by pyrolysis of hickory and oak woods. Given the limitations of the quantification approach employed by the applicant, the Panel could not judge whether the applied methods meet the legal quality criterion that at least 80% of the volatile fraction shall be identified and quantified. At the maximum proposed use levels, dietary exposure estimates calculated with DietEx ranged from 0.02 to 4.6 mg/kg body weight (bw) per day at the mean and from no dietary exposure to 13.0 mg/kg bw per day at the 95th percentile. The Panel concluded that four components in the Primary Product raise a potential concern for genotoxicity. In addition, a potential concern for genotoxicity was identified for the unidentified part of the mixture. The Primary Product contains furan‐2(5H)‐one and benzene‐1,2‐diol, for which a concern for genotoxicity was identified in vivo upon oral administration. Considering that the exposure estimates for these two components are above the threshold of toxicological concern (TTC) of 0.0025 μg/kg bw per day for DNA‐reactive mutagens and/or carcinogens, the Panel concluded that the Primary Product raises concern with respect to genotoxicity.

Details

Language :
English
ISSN :
18314732
Volume :
21
Issue :
11
Database :
Directory of Open Access Journals
Journal :
EFSA Journal
Publication Type :
Academic Journal
Accession number :
edsdoj.4dae2f8201c451e999fed7dbbdee634
Document Type :
article
Full Text :
https://doi.org/10.2903/j.efsa.2023.8364