Class ITerminated in FDA datasetRecall initiated Dec 22, 2014

Strawberry Basil ice cream, labeled in part, "***Full Tilt ice cream Strawberry Basil***

Recalling firm: Full Tilt Ice Cream

Why it was recalled

Full Tilt Brand ice cream is being recalled due to the potential to be contaminated with Listeria monocytogenes. These products contain ice cream mix, an ingredient manufactured…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 23, 2015.

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ProductStrawberry Basil ice cream, labeled in part, "***Full Tilt ice cream Strawberry Basil***Ingredients: Cream, milk, skim milk powder, sugar, Strawberries, basil, corn syrup solids, carob bean gum, guar gum, soy lecithin, carrageenan***Seattle WA 98106 www.fulltilticecream.com***". Ice cream is packaged in 16 oz paper containers, and 1.5 gallon and 3 gallon plastic tubs. UPC code: 713757814324
Package size16 oz
UPC713757814324

FDA code information

All products are coded with 7 digit code ending in 14x (ie: 0219142) produced before 12/19/2014.

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Full FDA record and distribution details

Original product description

Strawberry Basil ice cream, labeled in part, "***Full Tilt ice cream Strawberry Basil***Ingredients: Cream, milk, skim milk powder, sugar, Strawberries, basil, corn syrup solids, carob bean gum, guar gum, soy lecithin, carrageenan***Seattle WA 98106 www.fulltilticecream.com***". Ice cream is packaged in 16 oz paper containers, and 1.5 gallon and 3 gallon plastic tubs. UPC code: 713757814324

Extracted codes and context

TypeCode / valueContext
UPC713757814324in 16 oz paper containers, and 1.5 gallon and 3 gallon plastic tubs. UPC code: 713757814324

Original FDA recall reason

Full Tilt Brand ice cream is being recalled due to the potential to be contaminated with Listeria monocytogenes. These products contain ice cream mix, an ingredient manufactured and recalled by Snoqualmie Gourmet Ice Cream, Inc.

Recall details

Recall number
F-1056-2015
Event ID
70158
FDA status
Terminated
Initiated
Dec 22, 2014
Reported
Feb 18, 2015
Classified
Feb 10, 2015
Terminated
Feb 23, 2015
Quantity
177 cases, 6 per case
Location
Seattle, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distributed nationwide.

FDA source record · F-1056-2015

Data updated September 16, 2026. View official FDA data ↗

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