The Recall Desk
Agency classClass IOur severity:SevereFDA (Food)·F-1645-2023·Announced 2023-10-04

Razzle Bomb ice cream recalled for Listeria monocytogenes contamination

Ice Cream House is recalling Razzle Bomb ice cream products sold in Ohio, New Jersey, and New York due to potential contamination with Listeria monocytogenes.

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: FDA Class I classification requires a minimum severity score of 4. The recall involves Listeria monocytogenes, a high-risk pathogen.

Plain-English summary

Ice Cream House is recalling Razzle Bomb ice cream products. The recalled products include 8'' Razzle Bomb (UPC 0-91404-15421-5, dairy/parve) and 6'' Razzle Bomb (UPC 0-91404-15422-2, dairy/parve). These products were distributed in Ohio, New Jersey, and New York.

The products may be contaminated with Listeria monocytogenes. Consumers should not consume the recalled products and should return them to the place of purchase or discard them.

The recalled product

Product
8'' Razzle Bomb; dairy / parve; 1 PACK; UPC: 0-91404-15421-5 6'' Razzle Bomb; dairy / parve; 1 PACK; UPC: 0-91404-15422-2
Manufacturer
ICE CREAM HOUSE

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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