RecallRadar
ModerateReported June 17, 2026 (2 weeks ago)

NEURO NOURISH dietary supplement

Recalled by SENSORY SUPPLEMENT LLC

Food recall

SENSORY SUPPLEMENT LLC

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

SENSORY SUPPLEMENT LLC has recalled NEURO NOURISH dietary supplement, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on June 17, 2026 and was initiated on May 6, 2026. 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 NEURO NOURISH dietary supplement, with approximately 512 units affected. The company behind the recall is SENSORY SUPPLEMENT LLC, based in Beverly Hills, CA. The FDA describes the product as: “NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANTIOXIDANT NUTRITIONAL SUPPLEMENT TO SUPPORT DRAIN AND GUT HEALTH NET WT. 5.9 OZ; UPC: 310M5951601”

Why was NEURO NOURISH dietary supplement recalled?

According to the FDA, the stated reason for the recall is: “Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.”

What should you do?

If you think you may have bought NEURO NOURISH dietary supplement, compare it against the product description and identifying codes (LOT number: 310M5951601 Expiration: 0250A6 EXP 03/2028) 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 SENSORY SUPPLEMENT LLC or your local health authority.

About this recall

This recall was distributed in CA. 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.

Full recall details

Status
Ongoing
Date reported
June 17, 2026
Recall started
May 6, 2026
Distributed in
CA
What was recalled
NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANTIOXIDANT NUTRITIONAL SUPPLEMENT TO SUPPORT DRAIN AND GUT HEALTH NET WT. 5.9 OZ; UPC: 310M5951601
Why it was recalled (as stated by the FDA)
Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.
How to identify the affected product
LOT number: 310M5951601 Expiration: 0250A6 EXP 03/2028
Amount recalled
512 units

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 NEURO NOURISH dietary supplement recalled?+

According to the FDA: Premature lipid oxidation causing quality issue potentially causing product to have an off odor a…

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 NEURO NOURISH dietary supplement?+

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.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-1109-2026. Information last synced from the FDA on July 6, 2026.