CLASS II Food recall · Reported 3 Sep 2025 · FDA Enforcement Report

Carton Label: "Friendly's Vanilla Bean"; Lid Label recalled

DFA Dairy Brands is recalling Carton Label: "Friendly's Vanilla Bean"; Lid Label: "Friendly's Cookies and Cream", distributed in Maryland, Pennsylvania, Virginia. The recall was initiated on 1 Aug 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesExpiration Date: 11/26/25
Quantity recalled54 cases (324 individual containers)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0537-2025
FDA event ID
97389
Recalling firm
DFA Dairy Brands, Wilbraham, MA
Classification
Class II
Status
Terminated
Recall initiated
1 Aug 2025
FDA classified
27 Aug 2025
Reported
3 Sep 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Product category
Cookies

Timeline

1 Aug 2025Recall initiated by company
27 Aug 2025Classified by FDA+26 days
3 Sep 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product contains undeclared wheat and soy.

Product as listed by the FDA

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

Where it was distributed

MD, VA, PA

MarylandPennsylvaniaVirginia

Questions about this recall

Why was it recalled?

Product contains undeclared wheat and soy.

Which lots are affected?

Expiration Date: 11/26/25

Where was it sold?

MD, VA, PA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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