Food & Beverage Litigation & Regulatory Update

Tag: FDA

  • 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…

  • 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…

  • 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…

  • 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…

  • FDA Releases Food Guidance Priorities List

    The U.S. Food and Drug Administration (FDA) has released a list of the draft and final guidance topics that the agency is prioritizing for 2022. The list includes guidance on allergens, cell-cultured foods, heavy metals in juice and labeling of plant-based alternatives to milk and animal-derived foods. According to a caveat in the constituent update,…

  • Advocacy Groups Urge FDA to Ban Food Additive Use of BPA

    Several advocacy groups, including the Environmental Defense Fund, Consumer Reports and Environmental Working Group, have filed a petition with the U.S. Food and Drug Administration (FDA) “requesting that the agency remove its approvals of the use of bisphenol A [BPA] . . . because recently published scientific studies show that the exposure from those food additive…

  • FDA Revokes French Dressing Standard of Identity

    The U.S. Food and Drug Administration (FDA) has revoked the standard of identity for French dressing following a citizen petition filed by the Association for Dressings and Sauces. The revocation finalizes a December 2020 rule that “will allow for greater innovation and more flexibility of products on the market,” according to an FDA Constituent Update.…

  • Warning Letter Provides Insight on FDA’s Priorities

    By Of Counsel John Johnson III The U.S. Food and Drug Administration’s (FDA) Warning Letter to Maribel’s Sweets, Inc., provides an important look into how FDA is implementing the Food Safety Modernization Act (FSMA)’s Preventive Control Rule. This is the requirement that a food facility must have and implement a written food safety plan to…