FDA Recalls Qunol Turmeric Supplements Over Mold Contamination

The recall affects over 42,000 bottles distributed nationwide.

Published on Feb. 7, 2026

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The U.S. Food and Drug Administration has announced a recall of Qunol Extra Strength Turmeric (1,000 mg) supplements due to the detection of mold in the raw materials used to manufacture the product. The recall affects approximately 42,740 bottles distributed to retail stores in 30 states, including CVS locations.

Why it matters

Consuming supplements contaminated with mold can potentially lead to temporary or medically reversible health effects, though serious outcomes are unlikely. The recall highlights the importance of quality control and safety measures in the supplement industry to protect consumer health.

The details

The recall involves 60-count and 120-count bottles with UPC codes 850184008428 and 850184008435. Affected products carry lot codes 12811C120 BIO7771, 12811C120BJ BIO7772, or 12811C60 BIO8281, with a best-by date of October 2028. Consumers are urged to stop using the product immediately and either dispose of it or return it to the place of purchase for a refund.

  • The FDA announced the recall on February 7, 2026.

The players

U.S. Food and Drug Administration

The federal agency responsible for protecting public health by regulating the safety of food, drugs, and other products.

Qunol

The manufacturer of the recalled turmeric supplements.

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What’s next

The FDA is advising consumers who have experienced any symptoms after consuming the affected Qunol turmeric supplements to consult a healthcare professional.

The takeaway

This recall underscores the importance of rigorous quality control measures in the supplement industry to ensure consumer safety. It serves as a reminder for consumers to be vigilant about the products they purchase and to report any adverse effects to the appropriate authorities.