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Lower risk Food recall · FDA · Published May 6, 2026

Sensory Supplement Recalls Neuro Nourish for Quality Issues

Sensory Supplement LLC recalls Neuro Nourish dietary supplement due to premature lipid oxidation causing off odors and bitter taste. Check your lot number.

🇺🇸 FDA recall #H-1109-2026FoodSensory Supplement ›
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Recalling firmSENSORY SUPPLEMENT LLC9440 Santa Monica Blvd · Beverly Hills, CA 90210-4610
✎ GovInfoNow plain-language explainer

Sensory Supplement LLC is recalling Neuro Nourish, a dietary supplement marketed to support drain and gut health. The recall addresses a quality issue caused by premature lipid oxidation, which may result in the product having an off odor and a bitter taste. This specific batch consists of 512 units sold nationwide through the company's online website. Read more at govinfonow.com/recall/6363-sensory-supplement-recalls-neuro-nourish-for-quality-issues.

Source Summary by GovInfoNow · govinfonow.com/recall/6363-sensory-supplement-recalls-neuro-nourish-for-quality-issues · Updated October 9, 2026 · Official notice: FDA #H-1109-2026

Cite this page

“Sensory Supplement Recalls Neuro Nourish for Quality Issues.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6363-sensory-supplement-recalls-neuro-nourish-for-quality-issues. Based on FDA recall #H-1109-2026.

Sensory Supplement LLC voluntarily recalled Neuro Nourish dietary supplement on May 6, 2026, the FDA said. The product may have an off odor and bitter taste due to premature lipid oxidation.

How to tell if you have it

  • Brand: Sensory Supplement
  • Product: Neuro Nourish Dietary Supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANTIOXIDANT
  • UPC: 310M5951601
  • Lot number: 310M5951601
  • Expiration: 03/2028

The hazard

The recall addresses premature lipid oxidation causing a quality issue that may result in an off odor and bitter taste. The FDA classified the recall as Class II.

Context

GovInfoNow's records show other recent recalls of similar products include Wellnov Joint Nourish Liquid Recall (2026-04-23) and Aonic Complete His. Dosage Liquid Supplement Recall (2026-01-15). Vital Nutrients Aller-C Recall occurred on 2026-03-27.

How to tell if you have this one

Check your bottle for the UPC code 310M5951601 and Lot number 310M5951601. Verify the expiration date is 03/2028 (marked as EXP 03/2028 on lot 0250A6). The product is a 5.9 oz nutritional supplement.

  • Brand
    Sensory Supplement
  • Category
    Food

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Product is available nationwide and sold through the firm's online website direct to consumers.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 42 days after the firm started it.

1. Firm started the recall: May 6, 202612. Published in FDA’s Enforcement Report: Jun 17, 202623. FDA classified it Class II: Jun 24, 202632026
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class II

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-1109-2026 (May 6, 2026)
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA