CLASS II ONGOING Food recall · Reported 4 Feb 2026 · FDA Enforcement Report

Qunol, Extra Strength Turmeric Capsule recalled

Quten Research Institiute is recalling Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771, BIO7772, distributed in 30 states. The recall was initiated on 16 Dec 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesPart Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281

Quantity recalledTurmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ ,10304, Turmeric 1000mg Capsule 120ct Veg. 29160

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: H-0418-2026
FDA event ID: 98211
Recalling firm: Quten Research Institiute, Pine Brook, NJ
Brand: Qunol
Classification: Class II
Status: Ongoing
Recall initiated: 16 Dec 2025
FDA classified: 23 Jan 2026
Reported: 4 Feb 2026
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Mold
Product category: Herbal Supplements

Timeline

16 Dec 2025	Recall initiated by company
23 Jan 2026	Classified by FDA	+38 days
4 Feb 2026	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

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,

Alabama California Colorado Connecticut Delaware Florida Georgia Iowa Illinois Indiana Kentucky Louisiana Massachusetts Michigan Minnesota Missouri North Carolina New Jersey Nevada New York

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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

Where was it 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 should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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