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FDA and FTC Issue Warning Letters to CBD Companies

Posted on April 7, 2022

On March 28, 2022, the Food and Drug Administration (FDA) and Federal Trade Commission (FTC) jointly issued seven warning letters to companies marketing cannabidiol (CBD) products with COVID-19 related claims.

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FDA & FTC Issue Warning Letters to 10 Companies

Posted on September 14, 2021

On September 9, 2021, the Food and Drug Administration (FDA) and Federal Trade Commission (FTC) jointly issued warning letters to 10 companies for illegally selling dietary supplements claiming to treat

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FDA Issues Company-Wide Warning Letter Re Pet Food

Posted on August 20, 2021

FDA issued a corporate-wide warning letter to Midwestern Pet Foods, Inc. (Midwestern) on August 9, 2021. The letter states that inspections of the company’s pet food manufacturing plants revealed violations

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FDA Warns Companies over Unapproved Fertility Claims

Posted on May 27, 2021

On May 26, FDA published a constituent update informing the public that it has issued warning letters to five companies for marketing dietary supplements that claim to cure, treat, mitigate,

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FDA Issues Two Warning Letters for Undeclared Allergens

Posted on May 5, 2021

On May 4, the FDA published two Warning Letters for undeclared allergens and the “introduction or delivery for introduction into interstate commerce of any food that is misbranded” which is

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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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FDA Issues Warning Letters to Companies Selling CBD Products for Pain Relief

Posted on March 23, 2021

Last week the FDA issued warning letters to Honest Globe, Inc. (March 15, 2021) and Biolyte Laboratories, LLC (March 18, 2021) for selling products containing cannabidiol (CBD) in violation of

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FDA Warnings Against Supplements for Depression

Posted on February 22, 2021

FDA will evaluate claims and other information on a dietary supplement’s website to establish the product’s “intended use.” In general, a dietary supplement is allowed to make claims about having

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FDA Places All Alcohol-Based Hand Sanitizers from Mexico on Import Alert

Posted on January 27, 2021

On January 26, FDA placed all alcohol-based hand sanitizers from Mexico on a countrywide import alert in an effort to stop violative products from entering the US market until the

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FDA Issues Warning Letters to Vape Companies that Did Not Submit Premarket Tobacco Product Applications (PMTAs)

Posted on January 21, 2021

On January 15, 2021, the U.S. Food and Drug Administration (FDA) issued warning letters to ten companies that sell electronic nicotine delivery system (ENDS) products, including e-liquids. FDA’s letters warned

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