HIGHFDA FOOD

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.

Official notice
QUTEN RESEARCH INSTITIUTEFood & BeveragesPart Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA FOOD
Recall date
December 16, 2025
Status
ACTIVE
Severity
8/10

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Food Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
QUTEN RESEARCH INSTITIUTE
Product type
Turmeric Capsule
Model numbers
Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281
Sold at
Multiple Retailers
Where affected
Nationwide

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    December 16, 2025

  2. Reported by FDA FOOD

    February 4, 2026

  3. RecallRadar source check

    February 11, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

Qunol Extra Strength Turmeric Capsules are marketed as dietary supplements that support joint health and inflammation reduction. Consumers typically buy these capsules to incorporate turmeric's health benefits into their daily routines.

Why This Is Dangerous

Mold contamination in dietary supplements can occur during production or storage, leading to potential health risks if consumed. Mold can produce allergens and mycotoxins that can affect respiratory and gastrointestinal health.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall may cause inconvenience for consumers relying on these supplements for health benefits. Immediate action is necessary to avoid potential health risks associated with mold consumption.

Practical Guidance

How to identify if yours is affected

  1. Check the label for lot numbers BIO7771, BIO7772, or BIO8281.
  2. Look for the production date in July 2025 on the packaging.
  3. Verify the supplement count: 60, 120 count bottles.

Where to find product info

Lot numbers and production dates are typically found on the bottom or side of the bottle.

What timeline to expect

Expect a refund processing timeline of approximately 4-6 weeks.

If the manufacturer is unresponsive

  • Follow up with QUTEN RESEARCH INSTITUTE LLC via email or telephone.
  • Document all interactions and requests.

How to prevent similar issues

  • Purchase from reputable brands with quality assurance.
  • Look for third-party testing certifications.
  • Read product labels carefully for safety warnings.

Documentation advice

Keep records of your purchase and any correspondence with the manufacturer, including dates and details of the issue.

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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.

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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