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    • New Twist In “Natural” LawsuitSeptember 7th, 2011

      By Riëtte van Laack – On August 24, 2011, another class action suit regarding “natural” food labeling claims was filed in the Southern District of California.  The defendants include Kashi Co. (“Kashi”) and its general manager, as well as Kashi’s parent Kellogg Co. and its President …

    • NRDC Doggedly Pursues Action on BPAAugust 29th, 2011

      By Ricardo Carvajal – In June, we reported that the DC Circuit Court of Appeals decided it lacked exclusive jurisdiction over a Natural Resources Defense Council (“NRDC”) citizen petition seeking FDA action against BPA.  Undeterred, NRDC has now filed its complaint in district court.  The complaint …

    • FDA Maintains That Preparation of an NDI Notification Takes 20 HoursAugust 25th, 2011

      By Riëtte van Laack – Under the law, a manufacturer of a new dietary ingredient ("NDI") or a dietary supplement containing an NDI must notify FDA of the basis for the manufacturer’s conclusion that its product “will reasonably be expected to be safe.”  FDA’s regulation, 21 …

    • Del Monte Fresh Sues FDA to Invalidate Cantaloupe Import AlertAugust 23rd, 2011

      By Ricardo Carvajal – Del Monte Fresh Produce N.A., Inc. ("Del Monte Fresh") sued to invalidate an FDA import alert on cantaloupe from Productos Agricolas de Oriente, S.A. ("PAO"), a Guatemalan producer that is one of Del Monte Fresh’s principal suppliers.  FDA imposed the import alert …

    • Congressional Leaders Request FDA to Exclude Grocery Stores from Menu Labeling RequirementsAugust 18th, 2011

      By Cassandra A. Soltis – In response to the Food and Drug Administration’s (“FDA’s”) proposed rule on nutrition labeling of standard menu items in restaurants and similar retail food establishments, members of the U.S. Senate and House of Representatives have requested that FDA exclude grocery stores …

    • FDA Provides Another Chance to Comment on Its Proposal to Amend the Phytosterols Health ClaimAugust 14th, 2011

      By Riëtte van Laack – FDA is reopening the comment period on the proposed rule it published on December 8, 2010, to amend the regulations on plant sterol/stanol esters and risk of coronary heart disease.  (See our previous post on the proposed rule.) One of FDA’s proposed …

    • FDA Reopens Comment Period for Gluten-Free Labeling of FoodsAugust 4th, 2011

      By Cassandra A. Soltis – The Food and Drug Administration (“FDA”) has reopened the comment period for its proposed rule on “gluten-free” labeling of food to announce the availability of, and seek comments on, its report titled “Health Hazard Assessment for Gluten Exposure in Individuals with …

    • IFT Requests Proposals for Its Wellness 2012 ConferenceAugust 2nd, 2011

      The Institute of Food Technologists (“IFT”) is requesting proposals for its March 28-29, 2012 annual Wellness Conference, which will explore new trends and examine recent scientific, technological, and business information in the health and wellness sector of the food industry.  The conference will cover a …

    • Domestic Food Facilities, U.S. Agents, and Importers: Get Ready for FSMA FeesJuly 31st, 2011

      By Ricardo Carvajal – FDA announced fee rates for reinspections of domestic and foreign facilities, importer reinspections, and noncompliance with a recall order – all authorized by the Food Safety Modernization Act ("FSMA").  The fees kick in on October 1, 2011.  The hourly fee rate is …

    • 2 = 2, Unless the 2 are in “ONE A DAY”July 28th, 2011

      By Ricardo Carvajal – A federal district court dismissed with prejudice a claim that Bayer’s labeling of gummy vitamins violated the Arkansas Deceptive Trade Practices Act.  Plaintiff alleged that the brand name “ONE A DAY” is misleading because the daily serving size for the vitamins is …

    • HP&M Requests One-Year Comment Period for Draft NDI GuidanceJuly 26th, 2011

      On July 26, 2011, Hyman, Phelps & McNamara, P.C. filed a request for a one-year comment period to allow affected businesses adequate time to respond to a lengthy and controversial draft guidance on New Dietary Ingredient ("NDI") notifications that FDA issued earlier this month.  Our …

    • Can Efforts to Develop an Integrated Food Safety System Advance in the Face of State Budget Crises?July 19th, 2011

      By Ricardo Carvajal – The integration of federal and state food safety systems is one of the goals of the Food Safety Modernization Act.  To that end, FDA recently announced the availability of grant funding to help with the “design, development, delivery, and maintenance of a …

    • FDA’s NDI Guidance and the 18-Year Cycle of Correcting Regulatory OverreachJuly 14th, 2011

      By Wes Siegner, Ricardo Carvajal & Riëtte van Laack – Since at least the early 1960s, FDA has attempted to exercise control over the dietary supplement market, sometimes in ways that the public, industry and Congress have found unacceptable.  In the 60s, FDA proposed a regulation …

    • Will the Dog Days of Summer Offer a Reprieve to FDA and the Regulated Industry (and Your Bleary-Eyed Bloggers)? DoubtfulJuly 6th, 2011

      By Kurt R. Karst –     Over the Independence Day holiday, in between the family BBQ and fireworks, we had a few minutes to reflect on what a hectic month June was for FDA and the regulated industry.  There were the decisions handed down by the U.S. …

    • Industry Front-of-Pack Labeling and “Bad Foods” Come Under Added ScrutinyJune 26th, 2011

      By Ricardo Carvajal – The New England Journal of Medicine published two articles bound to stoke more controversy in the battle over approaches to countering obesity.  A perspective piece authored by Dr. Kelly Brownell, Director of the Yale Rudd Center for Food Policy and Obesity, and …