RecallHawk
Class II Recall

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

QUTEN RESEARCH INSTITIUTE LLC

Summary

The FDA issued a Class II for Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 12 by QUTEN RESEARCH INSTITIUTE LLC. Reason: Mold contamination detected for raw material lots that were produced in July and used in finished goods..

Details

Source

Food Recall

External ID

H-0418-2026

Action Date

2026-02-04

Status

Ongoing

Category

food

Product Description

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

Lot/Code Info: Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281

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

Reason for Recall

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

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,

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-16

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (QUTEN RESEARCH INSTITIUTE LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does QUTEN RESEARCH INSTITIUTE LLC have FDA actions?

This is the only FDA action we have on record for QUTEN RESEARCH INSTITIUTE LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0418-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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