RecallHawk
Class II Recall

Carton Label: "Friendly's Vanilla Bean"; 48 fl. oz. Lid Label: "Friendly's Cookies and Cream" Product in carton is Co

DFA Dairy Brands, LLC

Summary

The FDA issued a Class II for Carton Label: "Friendly's Vanilla Bean"; 48 fl. oz. Lid Label: "Friendly's Cook by DFA Dairy Brands, LLC. Reason: Product contains undeclared wheat and soy..

Details

Source

Food Recall

External ID

H-0537-2025

Action Date

2025-09-03

Status

Terminated

Category

food

Product Description

Carton Label: "Friendly's Vanilla Bean"; 48 fl. oz. Lid Label: "Friendly's Cookies and Cream" Product in carton is Cookies and Cream.

Lot/Code Info: Expiration Date: 11/26/25

Quantity Affected: 54 cases (324 individual containers)

Reason for Recall

Product contains undeclared wheat and soy.

Distribution

MD, VA, PA

Type: Voluntary: Firm initiated

Recall Initiated: 2025-08-01

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 43 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (DFA Dairy Brands, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does DFA Dairy Brands, LLC have FDA actions?

This is the only FDA action we have on record for DFA Dairy Brands, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0537-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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