FDA recall record

Full Tilt Ice Cream Label reads in part "***Full Tilt Ice Cream Fudge Brownie recall — FDA F-2237-2017

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…

Class IIclassification
F-2237-2017official record ID
May 24, 2017report date

Recall record at a glance

Official recordF-2237-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmFull Tilt Ice Cream
Report dateMay 24, 2017
Recall initiation dateApr 25, 2017
Quantity2862 pints
LocationSeattle, WA, United States

Official 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.

Why the product was recalled

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.

Distribution information

Greater Seattle Washington area.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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