Dessert on Wheels Recalled Due to Listeria Contamination
Ice Cream House is recalling Dessert on Wheels products sold in Ohio, New Jersey, and New York because they may be contaminated with Listeria monocytogenes. Consumers should not consume the affected products.
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: This is an FDA Class I recall involving Listeria monocytogenes, a high-risk pathogen. FDA Class I designates products with a reasonable probability of causing serious adverse health consequences or death.
Plain-English summary
Ice Cream House is recalling Dessert on Wheels frozen desserts that were distributed in Ohio, New Jersey, and New York. The products may be contaminated with Listeria monocytogenes.
This frozen dessert product is available in both single and 4-pack configurations. Consumers who purchased this product should not consume it.
Consumers with the recalled product should discard it. For more information about this recall, contact the FDA or consult the official recall notice.
The recalled product
- Product
- Dessert on Wheels; dairy / parve; 4 PACK / SINGLE; UPC: 0-91404-15339-3
- Manufacturer
- ICE CREAM HOUSE
- Category
- Food — Frozen Desserts
- 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)
- No codes.
Distribution
Part of a larger recall action
This product is one of 80 recalled by ICE CREAM HOUSE 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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