Fresh Recalls

FDAClass II · Food · Recall H-1109-2026 · Recalled June 17, 2026

NEURO NOURISH dietary supplement recall — SENSORY SUPPLEMENT LLC

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
NEURO NOURISH dietary supplement
Company / brand
SENSORY SUPPLEMENT
Lot / serial / date codes
LOT number: 310M5951601 Expiration: 0250A6 EXP 03/2028
Distribution
Product is available nationwide and sold through the firm's online website direct to consumers.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: NEURO NOURISH dietary supplement

3. Open the official notice or contact

Official recall ID
H-1109-2026
Brand
SENSORY SUPPLEMENT
Classification
Class II
Units affected
512 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Beverly Hills, CA, United States
Firm address
9440 Santa Monica Blvd, N/A, 90210-4610

Identifying details (verbatim from the notice)

Product codes / lots
LOT number: 310M5951601 Expiration: 0250A6 EXP 03/2028
Distribution
Product is available nationwide and sold through the firm's online website direct to consumers.
Firm notified the public via
E-Mail
FDA event ID
99116
Recall initiated
May 6, 2026
FDA classified
June 24, 2026
FDA report date
June 17, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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