Over 42,000 bottles of Qunol Extra Strength Turmeric supplements are recalled for mold. Check lot codes and UPCs to see if your turmeric is affected; return or dispose if it is. The FDA notes this recall as Class II, meaning it may cause temporary health effects.
There’s an active recall on turmeric supplements sold in 30 states, according to the U.S. Food and Drug Administration (FDA). This is due to a mold contamination.
Approximately 42,740 bottles of Qunol Extra Strength Turmeric (1,000-milligram) are affected, which were distributed in retail stores, including CVS, 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.
The recalled supplements were sold in 60-count and 120-count bottles and contain UPCs “850184008428” and “850184008435,” respectively. They also have printed lot codes “12811C120 BIO7771,” “12811C120BJ BIO7772” or “12811C60 BIO8281” as well as a best-by date of “10/2028”
Check your turmeric capsules, and if it matches the recalled information, dispose of it or return to your place of purchase for a refund. The product is being recalled because mold was detected in the raw material used to make the supplements. If you are showing signs of illness after consuming the recalled turmeric, consult with a healthcare professional.
As of January 23, this recall has been classified as a Class II, meaning that taking the recalled supplement may cause “temporary” health effects. For questions about this recall, contact the FDA at 1-888-INFO-FDA (1-888-463-6332).