Mold Risk Prompts Urgent Recall of Turmeric Supplements—What to Know The product was sold in 30 states. Close Credit: yokeetod / Getty Images Key Points Quten Research Institute is recalling Qunol Extra Strength Turmeric Capsules due to possible mold contamination in the raw materials, according to the FDA. The recall affects 60- and 120-count bottles of 1,000-milligram capsules, totaling about 42,740 bottles.The recalled products were sold nationwide at major retailers like Walmart and CVS, as well as on the Qunol website. Specific UPCs, lot numbers, and expiration dates are included in the recall notice.The FDA classified the recall as Class II, meaning the supplements could cause temporary or medically reversible health effects. Consumers are advised to stop using the product immediately and return it for a refund. If you take turmeric supplements, check the label on the product. Quten Research Institute of Pine Brook, New Jersey, is recalling its Qunol Extra Strength Turmeric Capsules due to possible mold contamination, according to the U.S. Food and Drug Administration (FDA). The 1000-milligram capsules are packaged in 60- and 120- count plastic HDPE bottles with screw-on caps. About 42,740 bottles are affected. The product was distributed to retail stores, including Walmart and CVS, in Texas, Florida, California, North Carolina, Michigan, Minnesota, Virginia, New Jersey, Massachusetts, Ohio, Illinois, Alabama, Connecticut, Tennessee, New York, Missouri, Pennsylvania, Rhode Island, South Carolina, Oklahoma, Georgia, Wisconsin, Nevada, Indiana, Iowa, Colorado, Louisiana, Oregon, Kentucky, and Delaware. The capsules were also sold via the Qunol website. Don't Miss Daily Green Supplement Recall Expands Amid Reports of Salmonella Infections and Hospitalizations Over 80,000 Bottles of Mouthwash Recalled Nationwide—Is Yours Affected? According to a notice issued by CVS, the 60-count bottle has a UPC of 850184008428 and a lot number of 12811C60 B1O8281, with an expiration date of 10/2028. The 120-count bottle has a UPC of 850184008435 and lot numbers 12811C120 B1O7771 (with an expiration date of 10/2028) and 12811C120BJ BIO7772. Mold was detected in the raw material used to make the supplements, triggering the recall. The FDA has classified the recall as Class II, meaning that the supplements may cause “temporary or medically reversible adverse health consequences." Follow us to see more of our stories on Google. Follow Us On Google If you purchased the recalled capsules, immediately stop taking them and return the product to the place of purchase for a refund. Explore more: News Recall News