RecallHawk
Class I Recall

De'Lighting Frozen Dessert / Pre-Cut 12 Slices; parve; 1 PACK / SINGLE; UPC: 0-91404-15266-2

ICE CREAM HOUSE

Summary

The FDA issued a Class I for De'Lighting Frozen Dessert / Pre-Cut 12 Slices; parve; 1 PACK / SINGLE; UPC: 0-9 by ICE CREAM HOUSE. Reason: Products may be contaminated with Listeria monocytogenes..

Details

Source

Food Recall

External ID

F-1642-2023

Action Date

2023-10-04

Status

Terminated

Category

food

Product Description

De'Lighting Frozen Dessert / Pre-Cut 12 Slices; parve; 1 PACK / SINGLE; UPC: 0-91404-15266-2

Lot/Code Info: No codes.

Quantity Affected: N/A

Reason for Recall

Products may be contaminated with Listeria monocytogenes.

Distribution

OH, NJ, NY

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-22

Company

ICE CREAM HOUSE

Brooklyn, NY

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 0 food recalls issued in the same week, part of 0 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (ICE CREAM HOUSE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does ICE CREAM HOUSE have FDA actions?

ICE CREAM HOUSE has 0 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1642-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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