Velvet Ice Cream Company Recalls Vanilla Bean Tubs for Listeria Risk
Velvet Ice Cream Company is recalling specific lots of Velvet Vanilla Bean ice cream due to potential Listeria monocytogenes contamination.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
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 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class I, which mandates a severity score of at least 4 according to the rubric.
Plain-English summary
Velvet Ice Cream Company is recalling Velvet Vanilla Bean 3 Gallon Tubs because the product may be contaminated with Listeria monocytogenes. The recall involves Lot 21100 of the product.
The affected ice cream was distributed in Illinois, Indiana, Kentucky, Michigan, Ohio, South Carolina, West Virginia, Pennsylvania, and New York. Listeria monocytogenes is a pathogen that can cause serious illness, particularly in vulnerable populations.
Consumers who have purchased the affected product should check their freezers for the specific lot number and stop consuming the product if it matches the recall details.
The recalled product
- Product
- Velvet Vanilla Bean 3 Gallon Tub - 1 Tub per Case
- Manufacturer
- Velvet Ice Cream Company
- Category
- Food — Ice Cream
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot 21100
Distribution
Part of a larger recall action
This product is one of 56 recalled by Velvet Ice Cream Company 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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