Class IIOngoingVoluntary: Firm initiated
SENSORY SUPPLEMENT LLC: food recall H-1109-2026
SENSORY SUPPLEMENT LLC of Beverly Hills, CA recalled NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANTIOXIDANT… Reason: Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste. The FDA listed it as Class II in its Enforcement Report dated Jun 17, 2026; distribution: nationwide.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 512 units
- Reason for recall
- Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.
- Codes, lots and dates on the package
- LOT number: 310M5951601 Expiration: 0250A6 EXP 03/2028
- Distribution pattern
- Product is available nationwide and sold through the firm's online website direct to consumers.
- Recalling firm
- SENSORY SUPPLEMENT LLC, Beverly Hills, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 6, 2026 |
| Classified by the FDA | Jun 24, 2026 |
| Published in the Enforcement Report | Jun 17, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1109-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.