Breadman Bakery; Multigrain 24oz. Baked for Breaman-Melrose Bakery Inc.
Breadbox Co. recalled this product and the FDA reported the enforcement action on 3 September 2025 as Class II. The recall was initiated by the firm. Finished product label does not include allergen ingredient Sesame Seed.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Breadman Bakery; Multigrain 24oz. Baked for Breaman-Melrose Bakery Inc. UPC# 8 6000947952 4
- UPC
- 860009479524
- Reason for recall
- Finished product label does not include allergen ingredient Sesame Seed.
- Recalling firm
- Breadbox Co.
- Firm location
- Santa Fe Springs, California, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- H-0531-2025
- Quantity
- 52 loaves
- Distribution
- product was distributed to 7 retail locations in Los Angeles, CA.
- Initiated
- 22 July 2025
- Reported by FDA
- 3 September 2025
- Terminated
- 22 October 2025
- Firm notified by
- Product codes
- Expiration date 06/11/2025
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 3 months, from 22 July 2025 to termination on 22 October 2025. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 1 state, and the FDA published the enforcement report 6 weeks after the firm began the recall.
- Recalls of a bakery product run a median of 6 months, so this one was shorter than usual for its category. Bakery is overwhelmingly an allergen category rather than a pathogen one: baking is a kill step, but a bakery runs many recipes down shared lines, so the failure that recalls a bakery product is usually a label or a changeover.
Filed under bakery. A product can sit in more than one.
Other bakery recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Breadbox Co.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2024-07-10 | Breadman Raisin Bread, plastic bag, 16oz | Breadbox Co. | Undeclared milk allergen and undeclared Yellow No. 5 | Class II |
| 2024-07-10 | Breadman Brioche products in plastic bags: Brioche Toast, 2 lb. (1 loaf/bag), Brioche Buns, 40oz (10 buns/bag), Brioche Sliders, 50oz (25 sliders/bag), Brioche Hot Dog, 40oz (10 buns/bag) | Breadbox Co. | Undeclared Yellow No. 5 | Class II |
| 2024-07-10 | Breadman Jalapeno Cheese Bagels, plastic bag, 16oz | Breadbox Co. | Undeclared milk allergen | Class II |
All 4 records for Breadbox Co.
All 2025 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.