FDA recall H-0418-2026 · Feb 4, 2026
QUTEN RESEARCH INSTITIUTE LLC: Qunol recall
Product
Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle .
Reason for recall
Mold contamination detected for raw material lots that were produced in July and used in finished goods.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281
- Quantity
- Turmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ ,10304, Turmeric 1000mg Capsule 120ct Veg. 29160
- 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,
- Recalling firm
- QUTEN RESEARCH INSTITIUTE LLC, Pine Brook, NJ
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2025-12-16
Source: openFDA enforcement record H-0418-2026 · search recall number H-0418-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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