FDA Recalls Ice Cream Pie for Listeria Monocytogenes Contamination
ICE CREAM HOUSE is recalling 9-inch ice cream pies distributed in Ohio, New Jersey, and New York due to potential Listeria monocytogenes contamination. Consumers should not consume the product.
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. The severity rubric specifies that FDA Class I recalls are Critical (score 5), as the FDA's classification for Class I indicates the defect is likely to cause serious adverse health consequences or death.
Plain-English summary
The FDA has classified this recall as Class I. ICE CREAM HOUSE is recalling 9-inch ice cream pies (vanilla and chocolate flavors) with UPC 0-91404-15428-4 due to potential contamination with Listeria monocytogenes.
The affected products were distributed in Ohio, New Jersey, and New York.
Consumers who have purchased this product should not consume it. The product should be discarded immediately or returned to the place of purchase for a refund.
The recalled product
- Product
- 9'' Ice Cream Pie Vanilla / Chocolate; dairy / parve; 1 PACK; UPC: 0-91404-15428-4
- Manufacturer
- ICE CREAM HOUSE
- Category
- Food — Frozen Dessert
- 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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