RecallHawk
Class II Recall

1972 Banana Pudding Ice Cream, 3 GAL, UPC 0 75196 00556 6

House Of Flavors, Inc.

Summary

The FDA issued a Class II for 1972 Banana Pudding Ice Cream, 3 GAL, UPC 0 75196 00556 6 by House Of Flavors, Inc.. Reason: Undeclared soy lecithin.

Details

Source

Food Recall

External ID

H-0384-2026

Action Date

2026-01-21

Status

Completed

Category

food

Product Description

1972 Banana Pudding Ice Cream, 3 GAL, UPC 0 75196 00556 6

Lot/Code Info: Lot numbers: 22236, 23175, 24019, 24051, 25070, 25247

Quantity Affected: 2,388 units

Reason for Recall

Undeclared soy lecithin

Distribution

AL AZ CT GA IA IL IN KY MI MN MO NC NJ NY OH TN TX VA

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-12

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.

House Of Flavors, Inc. has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (House Of Flavors, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does House Of Flavors, Inc. have FDA actions?

House Of Flavors, Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0384-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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