FDA recall, , Moderate risk
Qunol Extra Strength Turmeric Capsules
Qunol Extra Strength Turmeric Capsules may contain mold contamination.
Summary by Recall Canary from the FDA notice
What happened
QUTEN RESEARCH INSTITIUTE LLC of Pine Brook, New Jersey is recalling Qunol Extra Strength Turmeric Capsule, 1000mg in HDPE bottles with caps, including 120 count bottles BIO7771 and BIO7772, and 60 count bottle BIO8281, because mold contamination was detected for raw material lots produced in July and used in finished goods.
The recall began December 16, 2025, and was added to the FDA's Enforcement Report on January 23, 2026.
The recalled products were distributed in 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 and Wisconsin.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Affected if its lot code is listed.
Qunol, Extra Strength Turmeric Capsule
- Strength
- 1000 mg
- Lot code
- 12811C120
- BIO7771
- 12811C120BJ
- BIO7772
- 12811C60
- BIO8281
Recall details
- Company began the recall
- Sold in
- 30 states
- Company
- QUTEN RESEARCH INSTITIUTE LLCPine Brook, New Jersey
- Hazard
- Contamination
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98211
- Recall number
- H-0418-2026
- Quantity recalled
- Turmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ ,10304, Turmeric 1000mg Capsule 120ct Veg. 29160
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
