THE HAMPTON GROCER Recall: Product may be contaminated with Salmonella.

🇺🇸 United States

1. August 14, 2026 - Recall initiated
2. September 9, 2026 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-1309-2026

Event ID

99656

Status

Ongoing

Classification

Class I

Company

THE HAMPTON GROCER

Product description

THE HAMPTON GROCER brand; Lacnola; SMALL BATCH LACTATION GRANOLA, 8oz, stand up pouches; NUTRIENT DENSE INGREDIENTS + MORINGA; SUPPORTS + PROMOTES HEALTHY LACTATION; INGREDIENTS Organic Gluten Free Oats Organic Maple Syrup Organic Pumpkin Seeds Organic Coconut Oil Almond Butter Almonds Organic Coconut Sugar Chocolate Chips (Cane Sugar, Unsweetened Chocolate, Cocoa Butter) Organic Ground Flaxseed Moringa Leaf Powder Pure Vanilla Extract (Water, Alcohol, Vanilla Bean Extractives) Cream of Tartar Baking Soda Salt; CONTAINS: TREE NUTS (ALMOND, COCONUTS); DISTRIBUTED BY: The Hampton Grocer Inc. Montauk, NY; MADE IN A FACILITY THAT PROCESSES TREE NUTS, PEANUTS, SESAME, AND SOY; UPC 8 50035 32455 4

Quantity

4,059 units

Reason

Product may be contaminated with Salmonella.

Recall initiation date

August 14, 2026

Report date

September 9, 2026

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

Nationwide

UPC, lot, and code information

Lot Code HGLC-102125 with expiration date 21OCT2026 Lot Code HGLC-021326 with expiration date 13FEB2027

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

September 14, 2026 ET

Responsible company: THE HAMPTON GROCER

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: September 14, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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