Category: FDA
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FDA to Research Use of “Healthy” Symbol
The U.S. Food and Drug Administration (FDA) has announced that it will conduct quantitative consumer research on the use of “voluntary symbols that could be used in the future to convey the nutrient content claim ‘healthy.’” The agency is simultaneously “developing a proposed rule that would update when manufacturers may use the ‘healthy’ nutrient content…
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Yogurt Standard of Identity Updated to Allow for Technological Advancements
The U.S. Food and Drug Administration (FDA) has issued a final rule amending the acceptable qualities of food labeled as yogurt. Under the rule, the standards of identity for lowfat and nonfat yogurt will be combined with the general definition; in addition, the list of allowable ingredients has expanded to include additional substances such as…
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FDA Issues Guidance on FSMA Enforcement
The U.S. Food and Drug Administration (FDA) has issued guidance indicating that it will not enforce particular provisions implementing the Food Safety Modernization Act (FSMA). “In certain situations the FDA has determined it is appropriate to take time to consider options, including rulemaking, to address concerns raised by stakeholders, while continuing to protect public health,”…
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OEHHA, FDA Issue Updates on PFAS
Regulations governing the use of per- and polyfluoroalkyl substances (PFAS) continue to evolve. In California, the Office of Environmental Health Hazard Assessment (OEHHA) announced the addition of perfluorooctanoic acid (PFOA), one type of PFAS, to the list of chemicals established under the state’s Safe Drinking Water and Toxic Enforcement Act of 1986 (Prop. 65). The…
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Genome-Edited Beef Low Risk, FDA Announces
The U.S. Food and Drug Administration has announced that it has “made a low-risk determination for the marketing of products, including food, from two genome-edited beef cattle and their offspring.” The agency determined that the product does not raise any safety concerns and that the product developer is not expected to pursue FDA approval before…
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DeLauro Calls for Investigation into FDA Response to Infant Formula Concerns
U.S. Representative Rosa DeLauro (D-Conn.) has written a letter to the Office of the Inspector General seeking “assistance in investigating whether the Food and Drug Administration (FDA) took prompt, appropriate, and effective action leading up to the recent recall involving powdered infant formula produced by Abbott Nutrition’s Sturgis, Michigan plant.” DeLauro indicates she is “concerned…
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Advocacy Groups File Petition on Nanomaterials in Infant Formula
The Center for Food Safety and International Center for Technology Assessment have filed a rulemaking petition urging the U.S. Food and Drug Administration to regulate the use of nanotechnology in infant formula. “These new materials can have fundamentally different properties from their bulk material counterparts—properties that also create unique human health and environmental risks—which create…
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Guidance Issued on Food Commodities with Chlorpyrifos Residues
Following the Environmental Protection Agency’s 2021 final rule revoking tolerances for residues of the pesticide chlorpyrifos in food, the U.S. Food and Drug Administration’s (FDA’s) Center for Food Safety and Applied Nutrition has issued guidance for industry on how the agency will enforce the rule, which sets the expiration date for the tolerances as February…