Vanilla Bean, Full Tilt Ice Cream, packaged in 16oz pre packed pints and 3 gallon tubs. UPC on pint containers only: 00
Summary
The FDA issued a Class II for Vanilla Bean, Full Tilt Ice Cream, packaged in 16oz pre packed pints and 3 gallo by Full Tilt Ice Cream, LLC. Reason: The ice cream mix did not meet pasteurization specifications..
Details
Source
Food Recall
External ID
F-0966-2021
Action Date
2021-09-22
Status
Terminated
Category
food
Product Description
Vanilla Bean, Full Tilt Ice Cream, packaged in 16oz pre packed pints and 3 gallon tubs. UPC on pint containers only: 00856962005283
Lot/Code Info: Product with a Julian date of 20621X and before. Tubs mark with the date of 7/26/21 and before
Quantity Affected: 500 pints and 100 tubs
Reason for Recall
The ice cream mix did not meet pasteurization specifications.
Distribution
distributed in WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-07-29
Company
Seattle, WA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 30 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Full Tilt Ice Cream, LLC has 13 FDA actions in our database, including 13 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Full Tilt Ice Cream, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Full Tilt Ice Cream, LLC have FDA actions?
Full Tilt Ice Cream, LLC has 13 FDA actions in our database, including 13 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0966-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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