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

Breadman Bakery recalled by Breadbox

Breadbox is recalling Breadman Bakery, distributed in California. The recall was initiated on 22 Jul 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesExpiration date 06/11/2025
Quantity recalled52 loaves

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-0531-2025
FDA event ID
97349
Recalling firm
Breadbox, Santa Fe Springs, CA
Classification
Class II
Status
Terminated
Recall initiated
22 Jul 2025
FDA classified
26 Aug 2025
Reported
3 Sep 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Allergens
Product category
Other

Timeline

22 Jul 2025Recall initiated by company
26 Aug 2025Classified by FDA+35 days
3 Sep 2025Published in enforcement report+8 days

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

Reason for recall

Finished product label does not include allergen ingredient Sesame Seed.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Breadman Bakery; Multigrain 24oz. Baked for Breaman-Melrose Bakery Inc. UPC# 8 6000947952 4

Where it was distributed

product was distributed to 7 retail locations in Los Angeles, CA.

California

Questions about this recall

Why was it recalled?

Finished product label does not include allergen ingredient Sesame Seed.

Which lots are affected?

Expiration date 06/11/2025

Where was it sold?

product was distributed to 7 retail locations in Los Angeles, CA.

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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