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FDA Class II Recall Targets NuNaturals Stevia and Monk Fruit Sweeteners After Label Swap

Affected customers have been notified after the FDA classified the mix-up as posing reversible health risks.

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Overview

  • NuNaturals began a voluntary recall on July 14 when it found Organic Pure Stevia and Pure Monk Fruit Sweetener had been packaged under each other’s labels.
  • The FDA elevated the recall to Class II on August 1, signaling possible temporary or medically reversible health effects from the mislabeled powders.
  • A total of 156 bottles—78 of each sweetener—were distributed to retailers across the United States before the error came to light.
  • NuNaturals reports no adverse health incidents and has directly contacted all purchasers of the affected lots.
  • Consumers are urged to verify product UPCs and lot numbers before use and reach out to NuNaturals for return or replacement instructions.