The European Food Safety Authority (EFSA) has launched two public consultations on draft guidance for feed additives. Issued by EFSA’s Panel on Additives and Products or Substances Used in Animal Feed (FEEDAP), the first draft document offers guidance “for the preparation of dossiers for the renewal of the authorization for feed additives.” Under Article 14 of Regulation (EC) No. 1831/2003, FEEDAP currently requires applicants to renew feed additive permits every 10 years by providing enough technical information to “enable an assessment to be made of additives based on the current state of knowledge.” The panel has also requested feedback on draft guidance stemming from its updated assessment “of the toxigenic potential of Bacillus species used in animal nutrition.” According to EFSA, “Bacillus species are used in animal production directly as microbial feed additives or as the source of other feed additives, notably enzymes,” although certain strains—such as those in the…
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The Food and Drug Administration (FDA) has issued a final rule that amends color additive regulations to provide for “the safe use of mica-based pearlescent pigments prepared from titanium dioxide and mica as color additives in distilled spirits containing not less than 18 percent and not more than 23 percent alcohol by volume but not including distilled spirits mixtures containing more than 5 percent wine on a proof gallon basis.” The action follows a petition filed by E. & J. Gallo Winery and takes effect July 15, 2013. See Federal Register, June 12, 2013.
The U.K. Food Standards Agency (FSA) has launched public consultations on two sets of proposed legislation, “The Contaminants in Food (England) Regulations 2013” and “The Food Additives, Flavourings, Enzymes, and Extraction Solvents (England) Regulations 2013.” The first set of regulations related to food contaminants will revoke the 2010 version and take into account new European Commission regulations regarding (i) “maximum levels for nitrate in foodstuffs”; (ii) “maximum levels for the presence of coccidiostats and histomonostats in food resulting from the unavoidable carry-over of these substances in non-targeted feed”; and (iii) under-enforcement of EU provisions providing for “the labeling of groundnuts, other oilseeds, derived products thereof and cereals.” The Contaminants in Food Regulations will also revoke “national legislation on mineral hydrocarbons in food and revoke and remake[] the provisions of the Erucic Acid in Food Regulations 1977.” The second set of regulations will consolidate “all legislation within [FSA’s] remit covering food…
The European Food Standards Authority (EFSA) has issued a priority list of food additives “for which scientific data are required to finalize their re-evaluation within deadlines established by European legislation.” Tasked with re-evaluating hundreds of food additives by 2020, EFSA’s Panel on Food Additives and Nutrient Sources Added to Food (ANS Panel) has asked member states and other stakeholders to provide the following information for 51 food additives: (i) “figures from industry on the amounts of these additives they report using in their products”; and (ii) “data derived from analyses indicating actual levels of these additives found in foods and drinks from national food authorities, research institutions, academia, food industry, and other stakeholders.” To meet the evaluation deadlines, the ANS Panel has divided food additives into groups “based on the availability of scientific data.” The panel will accept data related to the 15 additives in the first group—which includes β-apo-8’-…
The Cornucopia Institute (CI) has issued a report that questions the safety of food-grade or undegraded carrageenan, “a common food additive extracted from red seaweed.” Titled “Carrageenan: How a ‘Natural’ Food Additive is Making Us Sick,” the report claims that animal studies “have repeatedly shown that food-grade carrageenan causes gastrointestinal inflammation and higher rates of intestinal lesions, ulcerations, and even malignant tumors.” Distinguishing between undegraded and degraded carrageenan—which the report describes as “a potent inflammatory” processed with acid instead of alkali—CI emphasizes that even the food-grade version poses a health risk to consumers who ingest the additive in a wide variety of products, including dairy and dairy alternatives, deli meats, and prepared soups and broths. In particular, the report points to a 2001 literature review published by the National Institute of Environmental Health Sciences that purportedly warned against “‘the widespread use of carrageenan in the Western diet’ due to evidence…
The Robert Wood Johnson Foundation’s (RWJF’s) Healthy Eating Research (HER) panel has released a set of age-based “Recommendations for Healthier Beverages” that urge government buildings, workplaces and other public venues to increase the availability of water and unflavored milk as replacements for high-calorie beverages. Billed as “an advisory panel of prominent researchers, nutritionists and policy experts,” HER evidently arrived at its findings after reviewing “current beverage standards, recommendations, and guidelines from scientific bodies, national organizations, public health organizations, and the beverage industry.” HER has generally recommended that “water should be available and promoted in all settings where beverages are offered” and endorsed unflavored, low-fat and nonfat milk in age-appropriate portions as a way for children to get adequate amounts of calcium, vitamin D, potassium, and other nutrients. The panel would also permit the consumption of small amounts of 100 percent fruit juice—ranging from 0 to-4-ounce portions for preschool children and 0-to-8-ounce…
U.S. Sen. Debbie Stabenow (D-Mich), who chairs the Senate Committee on Agriculture, Nutrition and Forestry, has joined ranking committee member Thad Cochran (R-Miss.) and 31 other senators in asking U.S. Trade Representative Ron Kirk “to quickly address Russia’s new import ban on U.S. beef, poultry and turkey.” According to a February 19, 2013, news release, the ban stems “from Russia’s zero tolerance policy regarding ractopamine, a feed additive for livestock approved by both the U.S. Food and Drug Administration and the Codex Alimentarius Commission [CODEX].” In their letter to the trade representative, the senators claim that this “egregious” trade barrier would cost the U.S. economy $600 million annually and amount to an import ban in violation of the World Trade Organization’s (WTO’s) Sanitary and Phytosanitary Agreement. “The United States must do everything it can to defend its rights in both the WTO and CODEX and prevent non-science-based trading practices from…
Apparently motivated in part by an online petition started by a 15-year-old from Mississippi, PepsiCo has reportedly decided to remove brominated vegetable oil (BVO), a flame retardant, from Gatorade®. Sarah Kavanagh posted the petition on Change.org after she read about studies linking BVO to possible health effects, and it was signed by more than 200,000 who agreed with her call for its removal. Additional information about the petition appears in Issue 463 of this Update. The company will not remove BVO from Mountain Dew® products. A company spokesperson reportedly said that PepsiCo has been testing alternatives for about a year, but because it continues to believe that the ingredient is safe, was not going to change the formulation until the petition met with such a response. Kavanagh taped a segment for “The Dr. Oz Show” and visited The New York Times while she was in New York. When she learned about…
Health Canada has issued a notice of modification adding steviol glycosides derived from the stevia plant to its list of permitted sweeteners. After concluding a technical consultation published on July 31, 2012, in response to three separate food additive submissions, Health Canada has evidently agreed that “available data support the safety and efficacy of steviol glycosides when used as described.” The revised list of permitted sweeteners authorizes the use of steviol glycosides as a tabletop sweetener and as a food additive in a number of food categories, including those pertaining to breakfast cereals, confections, nut and peanut spreads, fruit spreads, sauces, beverages, baking mixes, desserts, chewing gum, and condiments. Health Canada has directed food labeling questions about the use of common names for steviol glycosides, such as “purified stevia extract” and “stevia leaf extracts,” to the Canadian Food Inspection Agency.
The Food and Drug Administration (FDA) has issued final rules amending food additive regulations pertaining to the use of ionizing radiation in the production, processing and handling of meat and poultry products. Promulgated at the request of the U.S. Department of Agriculture, the rules took effect on November 30, 2012. FDA requests written objections or requests for a hearing by December 31. The meat-product irradiation amendment would “provide for the safe use of a 4.5 kilogray (kGy) maximum absorbed dose of ionizing radiation to treat unrefrigerated (as well as refrigerated) uncooked meat, meat byproducts, and certain meat food products to reduce levels of foodborne pathogens and extend shelf life.” The poultry-irradiation amendment would “increase the maximum dose of ionizing radiation permitted in the treatment of poultry products, to include specific language intended to clarify the poultry products covered by the regulations, and to remove the limitation that any packaging used…
