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411 PRESS
WarningRecall #H-0418-2026Food

QUTEN RESEARCH INSTITIUTE LLC Recalls Qunol

QUTEN RESEARCH INSTITIUTE LLC · Class II — Moderate Risk

Packaged food on grocery store aisle shelves — representative photo for FDA food recall
A U.S. grocery store aisle (representative file photo). Specific recalled product: see recall details below. Photo: Tessa Bury / Wikimedia Commons (CC BY 4.0).

Product Description

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

Reason for Recall

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

FDA Classification

Class II — Moderate Risk

A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

Distribution

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,

Remedy

Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.

411 Press Analysis

The FDA classified this recall as Class II, indicating the food product may cause temporary health problems or poses a slight threat of a serious nature. QUTEN RESEARCH INSTITIUTE LLC initiated the recall on December 16, 2025 affecting Turmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ,10304, Turmeric 1000mg Capsule 120ct Veg. 29160. Mold contamination detected for raw material lots that were produced in July and used in finished goods. The product was distributed nationwide. Consumers should check their purchases and discontinue use of any affected product. Contact QUTEN RESEARCH INSTITIUTE LLC for further instructions.

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