Breadman Bakery; Multigrain 24oz. Baked for Breaman-Melrose Bakery Inc. UPC# 8 6000947952 4
Summary
The FDA issued a Class II for Breadman Bakery; Multigrain 24oz. Baked for Breaman-Melrose Bakery Inc. UPC# 8 6 by Breadbox Co.. Reason: Finished product label does not include allergen ingredient Sesame Seed..
Details
Source
Food Recall
External ID
H-0531-2025
Action Date
2025-09-03
Status
Terminated
Category
food
Product Description
Breadman Bakery; Multigrain 24oz. Baked for Breaman-Melrose Bakery Inc. UPC# 8 6000947952 4
Lot/Code Info: Expiration date 06/11/2025
Quantity Affected: 52 loaves
Reason for Recall
Finished product label does not include allergen ingredient Sesame Seed.
Distribution
product was distributed to 7 retail locations in Los Angeles, CA.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-22
Company
Santa Fe Springs, CA
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.
Breadbox Co. 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 (Breadbox Co.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Breadbox Co. have FDA actions?
Breadbox Co. 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-0531-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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