Keto Farms LLC Recall: California Department of Public Health Inspection found that the allergen, coconut, was not declared on the label - F-2058-2019

🇺🇸 United States

1. August 8, 2019 - Recall initiated
2. August 28, 2019 - Reported by source
3. November 21, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2058-2019

Event ID

83534

Status

Terminated

Classification

Class II

Company

Keto Farms LLC

Product description

Keto Farms Keto Snack Mix - Tomato Pepperjack Fruit & Cheese Mix with Sprouted Pecans & Walnuts; Net Wt. 95 g (3.34 oz. Ingredients: Monterey Jack Cheese with Jalapeno Peppers, (Pasteurized Milk, Jalapeno Peppers, Cheese Culture, Salt, Enzymes), Sprouted Organic Walnuts, Sprouted Transitional Almonds, Grape Tomatoes, MCT Oil, Cold Water Sea Salt. Contains: Dairy (milk), Tree Nuts Made in USA: Distributed by: Keto Farms, Venice, CA 90291

Quantity

2,762 sellable units - total all varieties

Reason

California Department of Public Health Inspection found that the allergen, coconut, was not declared on the label

Recall initiation date

August 8, 2019

Report date

August 28, 2019

Classification date

Not published in this source record

Termination date

November 21, 2019

Distribution pattern

Nationwide and Canada, Australia, France, Great Britain and Mexico

UPC, lot, and code information

1000, 1001, 1003, 1004, 1005, 1006, 1007, 1008, 1009, 1010, 1011, 1012, 1013, 1014

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 83534 with 2 other product entries in Public Health Trace.

Responsible company: Keto Farms LLC

Other recalls from Keto Farms LLC

Where this information comes from

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

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

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

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." 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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of November 21, 2019.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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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