Velvet Ice Cream Recalls Super Dip Vanilla/Orange Ice Cream for Listeria
Velvet Ice Cream Company is recalling Super Dip Vanilla/Orange Ice Cream due to potential Listeria monocytogenes contamination. The product was distributed in nine states.
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 5/5 (Critical).
Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The recall is classified as FDA Class I, which indicates a reasonable probability that the use of, or exposure to, the violative product will cause serious adverse health consequences or death.
Plain-English summary
Velvet Ice Cream Company is recalling Super Dip Vanilla/Orange Ice Cream, 56oz Carton (4 Cartons per Case), due to the potential presence of Listeria monocytogenes. The recall affects Lot 21106.
The affected product was distributed in Illinois, Indiana, Kentucky, Michigan, Ohio, South Carolina, West Virginia, Pennsylvania, and New York.
Consumers should check their freezers for this specific product and lot number. If found, they should discard the product or return it to the place of purchase.
The recalled product
- Product
- Super Dip Vanilla/Orange Ice Cream 56oz Carton - 4 Cartons 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 21106
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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