Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap
Recalled by QUTEN RESEARCH INSTITIUTE LLC
Food recall
QUTEN RESEARCH INSTITIUTE LLC
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
QUTEN RESEARCH INSTITIUTE LLC has recalled Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on February 4, 2026 and was initiated on December 16, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, with approximately Turmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ… affected. The company behind the recall is QUTEN RESEARCH INSTITIUTE LLC, based in Pine Brook, NJ. The FDA describes the product as: “Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle .”
Why was Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap recalled?
According to the FDA, the stated reason for the recall is: “Mold contamination detected for raw material lots that were produced in July and used in finished goods.” In plain terms, this recall relates to mold.
Mold in food can affect its safety and quality, and some molds can produce compounds that make people unwell. Recalls for mold aim to remove affected products from shelves. Consumers are generally advised not to eat food that shows signs of spoilage.
What should you do?
If you think you may have bought Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, compare it against the product description and identifying codes (Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact QUTEN RESEARCH INSTITIUTE LLC or your local health authority.
About this recall
This recall was distributed in NJ. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Who this recall affects
This recall matters to anyone who bought Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap. Even if you feel fine, it's worth checking what you have on hand rather than assuming you were missed.
Distribution listed in the notice: 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 mold actually means
Mold in food can affect its safety and quality, and some molds can produce compounds that make people unwell. Recalls for mold aim to remove affected products from shelves. Consumers are generally advised not to eat food that shows signs of spoilage.
In this case, the concern applies specifically to Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap from QUTEN RESEARCH INSTITIUTE LLC — not to the wider category of products. Similar items from other brands aren't part of this recall.
How to check whether you have it
On packaged food, lot codes and best-by dates are usually printed in small date-coding ink on the side seam, the bottom of the package, or near the top seal — not on the front label. The UPC barcode is on the back or bottom.
Compare what you find against the identifying details in this recall: Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281
What to do if you already bought it
Do not eat the product, even if it looks and smells normal — contamination is usually invisible.
Return it to the store for a refund, or throw it away in a sealed bag so pets and wildlife can't reach it.
If it touched other food or surfaces, wash those surfaces and your hands with hot soapy water. When in doubt, contact QUTEN RESEARCH INSTITIUTE LLC or your local health department.
Full recall details
- Status
- Ongoing
- Date reported
- February 4, 2026
- Recall started
- December 16, 2025
- Distributed in
- NJ
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap recalled?+
According to the FDA: Mold contamination detected for raw material lots that were produced in July and used in finished…
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0418-2026. Information last synced from the FDA on October 10, 2026.