QUTEN RESEARCH INSTITIUTE LLC recalls Qunol
QUTEN RESEARCH INSTITIUTE LLC started this recall on December 16, 2025. The FDA classified it as Class II, a middle category: eating the product may cause temporary or medically reversible health problems, and serious harm is unlikely. It was distributed in 30 states. This recall is no longer considered active, but recalled products can stay in pantries and freezers for months.
- Status
- Closed / older
- Recall started
- December 16, 2025
- Company
- QUTEN RESEARCH INSTITIUTE LLC
- Classification
- Class II (temporary or reversible health risk)
- Where sold
- Alabama, California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Michigan, Minnesota, Missouri, North Carolina, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Virginia, Wisconsin
- Quantity
- Turmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ ,10304, Turmeric 1000mg Capsule 120ct Veg. 29160
Reason for recall (official wording)
Mold contamination detected for raw material lots that were produced in July and used in finished goods.
Recalled product (official wording)
- Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle .
Distribution
The product was distributed to the following states: TX, FL, CA, NC, MI, MN, VA, NJ, MA, OH, IL,AL, CT, TN, NY, MO, PA, RI, SC, OK, GA, MN, WI, NV, IN, IA, CO, LA, NC, OR, KY, DE,
What to do
Compare the brand, size, lot code and dates on your package with the details above. If they match, do not eat it. Throw it away or return it to the store. Contact a healthcare provider if you feel unwell. Step-by-step guide.
Source: FDA Enforcement Report (openFDA), event 98211.