The Recall Desk
Agency classClass IOur severity:SevereFDA (Food)·F-1680-2023·Announced 2023-10-04

Coffee Dessert Cups Recalled for Potential Listeria Monocytogenes Contamination

ICE CREAM HOUSE is recalling Coffee Dessert Cups due to potential Listeria monocytogenes contamination. The affected products were distributed in Ohio, New Jersey, and New York.

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: This is an FDA Class I recall. FDA Class I recalls for high-risk pathogens such as Listeria monocytogenes receive a minimum severity score of 4.

Plain-English summary

ICE CREAM HOUSE is recalling Coffee Dessert Cups due to potential contamination with Listeria monocytogenes. The recalled products are parve dessert cups sold in 6-pack or single servings with UPC 0-91404-15313-3.

The affected products were distributed in Ohio, New Jersey, and New York.

Consumers should not consume these products. They should discard them or return them to the store of purchase.

The recalled product

Product
Coffee Dessert Cups; parve; 6 PACK / SINGLE; UPC: 0-91404-15313-3
Manufacturer
ICE CREAM HOUSE
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

Distributed in 3 states:

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.

See all 80 products in this recall →

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