EFSA review of Maximum Residue Limits for halquinol in pig tissues as set by JECFA
In: EFSA supporting publications, Band 18, Heft 7
ISSN: 2397-8325
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In: EFSA supporting publications, Band 18, Heft 7
ISSN: 2397-8325
Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety and efficacy of 3‐phytase FLF1000 as a feed additive for pigs for fattening and minor porcine species for growing. This additive contains 3‐phytase produced by a genetically modified strain of Komagataella phaffii and it is authorised in the European Union as a feed additive for feed for chickens for fattening, laying hens, chickens reared for laying and for minor poultry species for fattening or reared for laying or for breeding. The applicant requested the extension of use of the additive to pigs for fattening and minor porcine species for growing. The FEEDAP Panel concluded that the use of the product as a feed additive for pigs raises no concerns for the consumer safety nor for the environment. The additive should be regarded as a potential respiratory sensitiser. The applicant provided a combined tolerance and efficacy trial in weaned piglets to support the safety for the target species. However, owing to the lack of precise data on the total feed intake of the animals, the FEEDAP Panel did not consider further the study for the assessment and consequently no conclusion could be drawn regarding the safety of the additive for pigs for fattening nor for other minor growing porcine species. Three studies were considered for the efficacy and from the data obtained the FEEDAP Panel concluded that the additive has the potential to be efficacious in improving the phosphorus utilisation in pigs for fattening at a minimum level of 500 FTU/kg feed.
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Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety and efficacy of Belfeed B MP/ML as a feed additive for sows in order to have benefits in piglets and for all porcine species. This additive contains endo‐1,4‐β‐xylanase produced by a genetically modified strain of Bacillus subtilis and it is authorised in the European Union as a feed additive for poultry for fattening, weaned piglets and pigs for fattening. The applicant requested the extension of use of the additive to sows in order to have benefits in piglets and to all porcine species at any developmental stage at 10 IU/kg feed. The FEEDAP Panel concluded that there are no concerns for consumer safety and no risks for the environment are expected from the use of Belfeed B MP/ML in all Suidae species. The additive is not irritant for skin or eye but it should be considered a potential respiratory sensitiser for the users, the Panel could not conclude on the potential of the additive as a potential dermal sensitiser. Considering the results from a tolerance trial done in weaned piglets, those in a subchronic oral toxicity study and the nature/origin of the product under assessment the Panel concluded that the additive is safe for all porcine species at any developmental stage. The data previously assessed in piglets and pigs for fattening allowed to conclude that the additive is efficacious at 10 IU/kg feed in suckling piglets and all Suidae species from suckling to slaughter. The data submitted to support the efficacy for sows was considered insufficient and therefore the Panel could not conclude on the efficacy in sows.
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In: EFSA journal, Band 21, Heft 10
ISSN: 1831-4732
In: EFSA journal, Band 21, Heft 10
ISSN: 1831-4732
In: EFSA journal, Band 17, Heft 2
ISSN: 1831-4732
In: EFSA journal, Band 22, Heft 10
ISSN: 1831-4732
Abstract
Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the safety and efficacy of lutein‐rich extract of Tagetes erecta L. as sensory additive (functional group: Colourants (ii) substances which, when fed to animals, add colours to food of animal origin) for turkeys for fattening. The additive is already authorised for use in feed for chickens for fattening and minor poultry for fattening and laying hens and minor poultry for laying. The FEEDAP Panel concluded that the use of lutein‐rich extract of T. erecta is safe for turkeys for fattening when used up to the maximum proposed use level of 80 mg total carotenoids/kg complete feed. The Panel concluded that the use of lutein‐rich extract of T. erecta in feed for turkeys for fattening under the proposed conditions of use would not be of concern for the consumer, considering also its use in other poultry for fattening and for laying hens. Regarding user safety, the lutein‐rich extract of T. erecta extract is irritant to skin and eyes and any exposure is considered a risk. The conclusions on user safety reached for the lutein‐rich extract of T. erecta would, in principle, apply to preparations made with it. The use of the additive in feed for turkeys for fattening under the proposed conditions of use is safe for the environment. The FEEDAP Panel concluded that the additive has the potential to colour the skin of turkeys for fattening at the proposed conditions of use.
In: EFSA journal, Band 22, Heft 10
ISSN: 1831-4732
Abstract
Following a request from the European Commission, the EFSA Panel on Nutrition, Novel Foods and Food Allergens (NDA) was asked to deliver an opinion on the safety of an extension of use of oil from Schizochytrium limacinum (strain FCC‐3204) as a novel food (NF) pursuant to Regulation (EU) 2015/2283. The extension of use pertains to the use of the NF as a food ingredient in protein products at a maximum use level of 1 g of docosahexaenoic acid (DHA) in 100 g of product. The Panel considers that the information provided on the composition and the production process is sufficiently described and does not raise safety concerns. S. limacinum was attributed the qualified presumption of safety (QPS) status with the qualification 'for production purposes only'. Data provided demonstrated the absence of viable cells in the NF. Under the proposed extension of use, the highest intake estimate (at the 95th percentile) of DHA from the NF in protein products is 6.3 mg DHA/kg bw per day for adolescents. The Panel notes that the exposure to DHA from the new intended use of the NF in protein products is very low compared to the exposure to DHA from the already authorised food categories (excluding food supplements). The Panel concludes that the NF (oil from S. limacinum (FCC‐3204)) is safe under the new intended use.
In: EFSA journal, Band 22, Heft 5
ISSN: 1831-4732
In: EFSA journal, Band 22, Heft 4
ISSN: 1831-4732
In: EFSA journal, Band 22, Heft 4
ISSN: 1831-4732
In: EFSA journal, Band 22, Heft 3
ISSN: 1831-4732
In: EFSA journal, Band 21, Heft 12
ISSN: 1831-4732
In: EFSA journal, Band 21, Heft 10
ISSN: 1831-4732
In: EFSA journal, Band 21, Heft 6
ISSN: 1831-4732