HIGH

Qunol Turmeric Capsules Recalled Due to Mold Contamination

Qunol recalled Extra Strength Turmeric Capsules due to mold contamination in raw materials. The recall affects over 3,000 units distributed across 27 states. Consumers should stop use and seek refunds immediately.

Quick Facts at a Glance

Recall Date
December 16, 2025
Hazard Level
HIGH
Brand
QUTEN RESEARCH INSTITIUTE
Category
Food & Beverages
Sold At
Multiple Retailers
Geographic Scope
Nationwide (50 states)
At-Risk Groups
GENERAL

Hazard Information

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

What You Should Do

Consumers who have purchased this product should not consume it. Contact QUTEN RESEARCH INSTITIUTE LLC for refund or replacement information. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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Product Details

The recall includes Qunol Extra Strength Turmeric Capsules in 1000mg. Affected models include BIO7771 (120 count), BIO7772 (120 count), and BIO8281 (60 count). These were produced in July 2025.

The Hazard

Mold contamination was detected in raw material lots of the turmeric capsules. Consumption could lead to potential health risks, thus the recall is classified as Class II.

What to Do

Consumers should stop using the affected turmeric capsules immediately. Contact QUTEN RESEARCH INSTITUTE LLC for refund or replacement information via email, fax, letter, or telephone.

Contact Information

For further assistance, reach QUTEN RESEARCH INSTITUTE LLC at their customer service number or visit their website. More details can also be found on the FDA enforcement report.

Key Facts

  • Recall date: December 16, 2025
  • Distribution states: TX, FL, CA, NC, MI, MN, VA, NJ, MA, OH, IL, AL, CT, TN, NY, MO, PA, RI, SC, OK,
  • Quantity recalled: 3,276 units
  • Lot numbers affected: BIO7771, BIO7772, BIO8281
  • Hazard classification: Class II

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281
Affected States
Nationwide
Report Date
February 4, 2026
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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