Taking effect by the 2026–2027 school year, the Arizona Healthy Schools Act has been signed into law, banning “ultra-processed foods,” defined as foods containing any one of 11 artificial food dyes and additives, from being sold in schools.
Arizona House Bill 2164, aiming to ban 11 chemicals and colorants, has passed the state House and has moved onto the Senate. Similar bills are currently progressing in West Virginia and Texas.
If FDA's regulatory decision-making should be based on science, but the Delaney Clause prohibits FDA from considering the totality of the available scientific evidence in making safety determinations for food and color additives, can the Delaney Clause and science-based decision making coexist?
Texas and West Virginia are the latest states to progress bills that aim to ban artificial food dyes and other additives from foods served at schools or from sale statewide.
In this episode of Food Safety Matters, we speak to Natalie Rainer and Dr. Peter Coneski, food regulatory experts at K&L Gates LLP, about the policy and legal issues surrounding food packaging chemicals of concern and targeted food additives, and the implications for industry.
If enacted during the New York State budget process in March, the Food Safety and Chemical Disclosure Act would require food companies to disclose their use of any “Generally Recognized as Safe” (GRAS) ingredients, and would ban some additives and dyes from foods sold or made in New York or in its schools.
This episode of Food Safety Five covers the U.S. Food and Drug Administration’s (FDA’s) recent ban on red dye 3, including the legal and scientific justifications for the decision, as well as external pressures from various parties leading to the ban.
In response to external pressures, FDA has revoked its authorization for the use of red dye 3 in food. Despite its decision, the agency maintains that the available scientific information does not support claims of the colorant being harmful to human health through dietary exposure.
This episode of Food Safety Five covers a recent amendment made to the EU microbiological criteria for managing Listeria monocytogenes in certain ready-to-eat foods. Also discussed are recent pressures put on FDA to ban red dye 3 in foods.
In a recent Senate hearing, top U.S. Food and Drug Administration (FDA) officials shared how resource constraints hinder its food chemical safety review work, and provided insight into a pending decision about red dye 3’s authorization for food use.
