Full Tilt Ice Cream Recall: Full Tilt Ice Cream is recalling pint size ice cream due to undeclared allergen, wheat. Flour is listed in the ingredient statement, however wheat is not declared.

🇺🇸 United States

1. April 25, 2017 - Recall initiated
2. May 24, 2017 - Reported by source
3. July 19, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2237-2017

Event ID

77133

Status

Terminated

Classification

Class II

Company

Full Tilt Ice Cream

Product description

Label reads in part "***Full Tilt Ice Cream Fudge Brownie Swirl Vegan***one pint***Ingredients: Coconut Milk (coconut milk, water, citric acid), organic evaporated cane juice, bownie bits (flour, sugar, cocoa powder, non-aluminum baking powder, salt, vanilla extract, coconut oil.), fudge (cocoa powder, unsweetened chocolate, sugar, cocoa fat, soy lecithin), vanilla extract guar gum***" Please note bownie is how this word appears on the label. UPC 6 96859 21161 4 The product is packed in paper pint containers with paper and plastic lid. Product is shrink wrapped six per flat (not in a cardboard case) and not packed in a master carton. Distributed as shrink wrapped, six pints per flat.

Quantity

2862 pints

Reason

Full Tilt Ice Cream is recalling pint size ice cream due to undeclared allergen, wheat. Flour is listed in the ingredient statement, however wheat is not declared.

Recall initiation date

April 25, 2017

Report date

May 24, 2017

Classification date

Not published in this source record

Termination date

July 19, 2017

Distribution pattern

Greater Seattle Washington area.

UPC, lot, and code information

116 16 through 114 17 Julian date Calendar year

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Full Tilt Ice Cream

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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