Whole Flower Farms LLC Recall: Peanut Butter Chocolate Chip Cookie product is recalled due to undeclared soy lecithin.

🇺🇸 United States

1. September 17, 2019 - Recall initiated
2. October 9, 2019 - Reported by source
3. September 30, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2256-2019

Event ID

83829

Status

Terminated

Classification

Class II

Company

Whole Flower Farms LLC

Product description

Peanut Butter Chocolate Chip Cookie, net wt. 2 oz. The product was distributed frozen and has a 5-day shelf life after being defrosted at the stores. The label is read in parts: "***Peanut Butter Chocolate Chip Cookie*** Ingredients: Peanut Butter, evaporated cane juice, brown sugar, sunflower oil, almond milk, chocolate chips, sorghum flour, white rice flour, tapioca starch, flax, vanilla, sea salt, baking soda***Gluten-Free ***Vegan Foods ***Made by: Whole Flower Farms 29190 hwy 34 Corvallis, OR***".

Quantity

20 units

Reason

Peanut Butter Chocolate Chip Cookie product is recalled due to undeclared soy lecithin.

Recall initiation date

September 17, 2019

Report date

October 9, 2019

Classification date

Not published in this source record

Termination date

September 30, 2019

Distribution pattern

distributed in Oregon.

UPC, lot, and code information

9/7/19 This date represents the production date.

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

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 83829 with 4 other product entries in Public Health Trace.

Responsible company: Whole Flower Farms LLC

Other recalls from Whole Flower Farms LLC

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: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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 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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