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ACTIVE RECALL — CLASS IIActive recallH-0418-2026/FDA enforcement
Quten Research Institiute LLC·Food·Dec 16, 2025

Qunol, Extra Strength Turmeric Capsule, 1000mg, Hdpe Bottle with Cap, BIO7771 120 Count Bottle, …

What you need to know

Class II

  • What happened

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

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Visible or laboratory-detected mold can signal a moisture, temperature or seal failure.

  • Action required

    Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.

Active recall · classified by the FDATX, FL, CA, NC +26 moreMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameQuten Research Institiute LLC
Recalling firmQuten Research Institiute LLCPine Brook, NJ, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281
Distribution area
TXFLCANCMIMNVANJMAOHILALCTTNNYMOPARISCOKGAWINVINIACOLAORKYDE

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,

United States

Quantity affectedTurmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ, 10304, Turmeric 1000mg Capsule 120ct Veg. 29160
Recall initiationFDA report date: February 4, 2026
FDA recall numberH-0418-2026

Beyond the headline

The recall, in context

Quten Research Institiute LLC initiated this food recall on December 16, 2025. The FDA enforcement report states: Mold contamination detected for raw material lots that were produced in July and used in finished goods. The FDA report lists distribution as: 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,.

The FDA enforcement report describes the reason as: Mold contamination detected for raw material lots that were produced in July and used in finished goods.

Qunol, Extra Strength Turmeric Capsule, 1000mg, Hdpe Bottle with Cap, BIO7771 120 Count Bottle, … was made or distributed by Quten Research Institiute LLC in Pine Brook, NJ, United States. This page reflects FDA report H-0418-2026, dated February 4, 2026.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, visible or laboratory-detected mold can signal a moisture, temperature or seal failure.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Mold contamination

Symptoms to watch for

Eating a moldy product may cause nausea, vomiting, diarrhea or allergic reactions. Do not intentionally inspect, smell or taste a suspect product.

Higher-risk groups

People with mold allergies, asthma, a weakened immune system, pregnant people and young children should be especially cautious.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Visible mold can indicate a moisture, packaging or temperature failure.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Qunol, Extra Strength Turmeric Capsule, 1000mg, Hdpe Bottle with Cap, BIO7771 120 Count Bottle, … recall?

Quten Research Institiute LLC recalled Qunol, Extra Strength Turmeric Capsule, 1000mg, Hdpe Bottle with Cap, BIO7771 120 Count Bottle, … in an FDA Class II enforcement action reported as H-0418-2026. Mold contamination detected for raw material lots that were produced in July and used in finished goods.

What should I do if I bought this product?

Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Is the Quten Research Institiute LLC recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0418-2026. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.