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Class II: temporary or reversible health riskOngoing

Quten Research Institiute Qunol Recall

Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count…

QUTEN RESEARCH INSTITIUTE LLC · Pine Brook, NJ

Risk level
Class II
Reported by FDA
Feb 4, 2026
Recall ID
H-0418-2026
Check your lot numberHow we source this data

Summary

Quten Research Institiute recalled Qunol starting Dec 16, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report H-0418-2026 on Feb 4, 2026. Reason: Mold contamination detected for raw material lots that were produced in July and used in finished goods. Status: Ongoing.

Why it was recalled

Mold contamination detected for raw material lots that were produced in July and used in finished goods.

Product description

Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle .

Lot numbers, UPCs & expiration codes

Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281

Where it was sold

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 if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0418-2026
Classification
Class II
Status
Ongoing
Recall initiated
Dec 16, 2025
FDA report date
Feb 4, 2026
Quantity
Turmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ ,10304, Turmeric 1000mg Capsule 120ct Veg. 29160
Recall type
Voluntary: Firm initiated
Recalling firm
QUTEN RESEARCH INSTITIUTE LLC

Original FDA data

Every field from FDA enforcement report H-0418-2026, exactly as published.

Show all FDA fields
City
Pine Brook
State
NJ
Status
Ongoing
Country
United States
Event ID
98211
Address
10 Bloomfield Ave
Code information
Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281
Postal code
07058-9743
Report date
Feb 4, 2026
Product type
Food
Recall number
H-0418-2026
Classification
Class II
Recalling firm
QUTEN RESEARCH INSTITIUTE LLC
Product quantity
Turmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ ,10304, Turmeric 1000mg Capsule 120ct Veg. 29160
Reason for recall
Mold contamination detected for raw material lots that were produced in July and used in finished goods.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle .
Distribution pattern
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,
Recall initiation date
Dec 16, 2025
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jan 23, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0418-2026, published Feb 4, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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