More Than 42,000 Bottles of Qunol Turmeric Supplements Recalled Over Mold Contamination in 30 States
More than 42,000 bottles of Qunol Extra Strength Turmeric supplements have been recalled across 30 states due to mold contamination, according to the U.S. Food and Drug Administration (FDA). The recall, which was initially announced in December 2025, was officially classified as a Class II event on January 23, 2026.
A Class II recall indicates that use of the affected product may cause temporary or medically reversible adverse health consequences, with a remote probability of serious health risks.
What Products Are Affected?
The recall impacts approximately 42,740 bottles of Qunol Extra Strength Turmeric, 1,000-milligram capsules. The supplements were sold in both 60-count and 120-count bottles at major retail locations, including CVS Pharmacy and Wegmans.
The affected products include:
60-Count Bottle
- Product Name: Qunol Extra Strength Turmeric 1000mg
- SKU: 300580
- UPC: 850184008428
- Lot Code: BIO8281 (also printed as 12811C60 BIO8281)
- Expiration Date: 10/2028
120-Count Bottle
- Product Name: Qunol Extra Strength Turmeric 1000mg
- SKU: 387443
- UPC: 850184008435
- Lot Codes: BIO7771, BIO7772 (also printed as 12811C120 BIO7771 and 12811C120BJ BIO7772)
- Expiration Date: 10/2028
Consumers are encouraged to check the UPC numbers, lot codes and expiration dates printed on their bottles to determine whether their product is included in the recall.
Where Were the Supplements Sold?
The recalled turmeric supplements were distributed in retail stores in the following states:
Alabama, California, Colorado, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kentucky, Louisiana, Massachusetts, Michigan, Minnesota, Missouri, Nevada, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Virginia and Wisconsin.
Why Were the Products Recalled?
The recall was initiated after mold was detected in the raw material used to manufacture the supplements. Mold contamination can pose health risks, particularly for individuals with compromised immune systems, mold allergies or respiratory conditions.
While the FDA’s Class II designation suggests that serious adverse health effects are unlikely, the agency notes that temporary health effects may occur in some individuals.
What Should Consumers Do?
Quten Research Institute, the manufacturer of the Qunol turmeric supplements, advises consumers who purchased the affected products to stop using them immediately.
Customers may return the recalled supplements to their place of purchase for a full refund. Alternatively, the products may be disposed of properly if returning them is not feasible.
Anyone experiencing symptoms of illness after consuming the recalled supplement should consult a healthcare provider. Consumers with questions about the recall can contact the FDA at 1-888-INFO-FDA (1-888-463-6332).
Ongoing Monitoring
The FDA continues to monitor supplement recalls as part of its oversight of dietary supplements sold in the United States. Consumers are encouraged to stay informed about recalls and regularly check lot numbers on supplement bottles, particularly for products purchased in late 2025.
Turmeric supplements are commonly used for their anti-inflammatory and antioxidant properties, but this recall underscores the importance of quality control in dietary supplement manufacturing and the need for consumers to remain vigilant about product safety.
