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Food & Beverage Litigation Update: Issue 631
  • Shook Hardy & Bacon LLP
  • USA, Canada, European Union
  • April 10 2017

The U.S. Food and Drug Administration (FDA) has announced an extension to its comment periods for information on the use of genome editing


The Uptick in FDA Warning Letters: What It Means for Cosmetics Manufacturers
  • Shook Hardy & Bacon LLP
  • USA
  • August 12 2016

The U.S. Food and Drug Administration (FDA) recently flexed its regulatory muscles in the cosmetics and personal care products industry by


FDA Issues Three Warning Letters to Marketers of Skin Care Products
  • Shook Hardy & Bacon LLP
  • USA
  • July 28 2016

The U.S. Food and Drug Administration (FDA) has issued three warning letters to companies marketing topical skin care products. According to these


FDA Investigates WEN by Chaz Dean Cleaning Conditioners after Adverse Event Reports
  • Shook Hardy & Bacon LLP
  • USA
  • July 28 2016

The U.S. Food and Drug Administration (FDA) posted a July 19, 2016, safety report warning of adverse event complaints concerning WEN by Chaz Dean


FDA Issues Warning Letter Regarding Lead in “Bentonite Me Baby” Topical Clay
  • Shook Hardy & Bacon LLP
  • USA
  • April 29 2016

The U.S. Food and Drug Administration (FDA) issued a warning letter on March 16, 2016, to Alikay Naturals over its "Bentonite Me Baby" product line


FDA Cracks Down on Dietary Drug Distributor
  • Shook Hardy & Bacon LLP
  • USA
  • March 24 2016

The U.S. Food and Drug Administration (FDA) issued a warning letter to Texas-based dietary supplement distributor Lucy's Weight Loss System, dba


Preemption Found in Another Drug MDL
  • Shook Hardy & Bacon LLP
  • USA
  • November 28 2015

Implied preemption makes complete sense when it is evident that the FDA would not have permitted label changes that plaintiffs in private litigation


American Egg Board campaigned against just Mayo, emails reveal
  • Shook Hardy & Bacon LLP
  • USA
  • September 17 2015

Weeks after the U.S. Food and Drug Administration (FDA) sent Hampton Creek Foods a letter warning that its Just Mayo is misbranded because it does


Regulators take aim at stimulant included in workout supplements
  • Shook Hardy & Bacon LLP
  • USA
  • July 1 2015

The U.S. Food and Drug Administration (FDA) recently sent several warning letters to manufacturers of over-the-counter supplement products that


FDA issues allergen labeling guidance
  • Shook Hardy & Bacon LLP
  • USA
  • June 19 2015

The U.S. Food and Drug Administration (FDA) has announced the availability of industry guidance on food allergen labeling exemptions. Titled "Food