Regulatory
FDA Recalls Gas-X, Generic Cymbalta, and Moringa Supplements
Key Facts
Signal Type
Regulatory
Industry
Biotech
Companies
Ascend Laboratories, LLC, Breckenridge Pharmaceutical, Fresenius Kabi USA, LLC, Zydus Pharmaceuticals (USA) Inc.
Date
June 15, 2026
The FDA issued nationwide recalls for Gas-X, generic Cymbalta (Duloxetine), and Moringa supplements. Ascend Laboratories, Breckenridge Pharmaceutical, Fresenius Kabi USA, and Zydus Pharmaceuticals are involved. Reasons include nitrosamine impurities, dissolution failures, and stability issues.
Consumers using Gas-X, Duloxetine, or Moringa supplements are directly impacted. Pharmacies and distributors carrying these products must manage returns and replacements. Manufacturers face potential reputational damage and financial losses.
Monitor FDA enforcement reports for updates on recalls and classifications. Watch for responses from affected companies, including corrective actions and communications to consumers. Track market reactions and shifts in consumer preferences.
Source:
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