Full Tilt Mint Chip Ice Cream Recall for Pasteurization Failure
Full Tilt Ice Cream is recalling Mint Chip ice cream in 3-gallon tubs distributed in Washington because the ice cream mix did not meet pasteurization specifications.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II recall involving inadequate pasteurization of a dairy product. Although no illnesses or injuries have been reported in the source text, inadequate pasteurization presents a risk of pathogenic contamination and foodborne illness, meeting the High severity threshold for risk-of-harm products without reported illness.
Plain-English summary
Full Tilt Ice Cream, LLC is recalling Mint Chip ice cream packaged in 3-gallon tubs because the ice cream mix did not meet pasteurization specifications.
The affected product was distributed in Washington. The recalled tubs are marked with a Julian date of 20621X and before, or a date of 7/26/21 and before on the tub.
Consumers who have purchased this product should not consume it. Consumers with questions or concerns should contact Full Tilt Ice Cream, LLC.
The recalled product
- Product
- Mint Chip, Full Tilt Ice Cream brand, packaged in 3 gallon tubs. No UPC.
- Manufacturer
- Full Tilt Ice Cream, LLC
- Category
- Food — Dairy / Ice Cream
- Affected units
- 75
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 13 recalled by Full Tilt Ice Cream, LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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