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The Daily Intake

Legal and Regulatory updates for the food and supplement industry

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Proposed Class Action Suit Against PepsiCo Regarding “No Preservatives” Label on Sparkling Juice Products

Posted on December 9, 2022

Pepsi Falsely Touts ‘No Preservatives’ In Izze Drinks, Suit Says (Subscription to Law360 required)

  • On December 1, PepsiCo and the equity firm behind Tropicana, PAI Partners, Inc., were named defendants

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Continue Reading Proposed Class Action Suit Against PepsiCo Regarding “No Preservatives” Label on Sparkling Juice Products

FDA Webinar on Action Levels for Lead in Juice

Posted on May 26, 2022
  • FDA will hold a webinar on Tuesday, June 14, 2022, at 1:00 pm (ET) to provide an overview of the recent draft guidance that the Agency issued on action levels

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FDA Issues Draft Action Levels for Lead in Juice

Posted on April 29, 2022
  • On April 27, 2022, FDA issued a draft guidance providing draft action levels for lead in single-strength apple juice and other single-strength juices. FDA states that the new levels are

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FDA Updates Guidance on Exemptions from FSMA

Posted on December 23, 2021
  • As previously reported on this blog, in 2017 FDA issued guidance documents on exemptions from FDA Food Safety Modernization Act (FSMA) rules to clarify which parts of the FSMA

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Exemptions Limited for Juice Preventive Controls

Posted on March 29, 2021
  •  FDA recently posted a March 5, 2021 Warning Letter to Panther James LLC for the manufacture of untreated juices without a Hazard Analysis and Critical Control Point (HACCP) plan and

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Federal Court Enters Consent Decree Against Juice Processor for Distributing Adulterated Juice

Posted on January 19, 2021

·      The U.S. District Court for the Eastern District of Washington has entered a consent decree between the FDA and Valley Processing, Inc. and the company’s owner and president, Mary …

Continue Reading Federal Court Enters Consent Decree Against Juice Processor for Distributing Adulterated Juice

FDA Issues Guidances on Exemptions from FSMA Rules

Posted on August 8, 2017
  • As previously reported on this blog, the U.S. Food and Drug Administration issued final rules to implement the hazard analysis and risk-based preventive control (HARPC) provisions under the FDA

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Recent Updates

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  • FSIS Proposes New Rules Regarding U.S. Origin Claims
  • FDA Issues Draft Guidance on Dietary Guidance Statements on Food Labels
  • California Assembly Members Introduce Bill to Ban Certain Color Additives
  • New Report Outlines FDA’s Strategy to Ensure the Safety of Imported Seafood

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Keller and Heckman, founded in 1962, has a broad practice in the areas of regulatory law, public policy, and litigation, serving both domestic and international clients. Our firm is a pioneer in the use of interdisciplinary approaches to problem-solving. Since 1971, we have had an in-house scientific staff that works closely with the firm’s attorneys on matters of technical complexity. Many of our attorneys also have government experience and expertise in multiple areas of the law.

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