Class IIOngoing in FDA datasetRecall initiated Jul 24, 2025

Wheat Hamburger Buns --- Ingredient Declaration: Water, Whole Wheat Flour, Enriched Wheat Flour…

Recalling firm: The Bonami Baking Company, Inc.

Why it was recalled

Undeclared milk and/or eggs from sub-ingredients and/or Contains statement.

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Compare the exact product and package details with the label you have.

ProductWheat Hamburger Buns --- Ingredient Declaration: Water, Whole Wheat Flour, Enriched Wheat Flour (Unbleached Wheat Flour, Malted Barley Flour, Niacin, Iron, Thiamin Mononitrate (Vitamin B1) Riboflavin (Vitamin B2), Folic Acid) Eggs, Butter (Pasteurized Cream, Natural Flavorings), Sugar, Water, Dried Whey, Salt, Yeast --- Contains Allergen: Wheat --- Heating Instructions: Remove Buns from freezer and defrost in refrigerator. Serve at room temperature or toast bun for 3-5 minutes in 350-degree oven for optimal flavor. --- Net weight: 27.00 LBS. (12 ct / 12 pkgs) --- The Bonami Baking Co.
Package size27.00 LBS

FDA code information

USE BY: 7/20/25 through 7/20/26

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Full FDA record and distribution details

Original product description

Wheat Hamburger Buns --- Ingredient Declaration: Water, Whole Wheat Flour, Enriched Wheat Flour (Unbleached Wheat Flour, Malted Barley Flour, Niacin, Iron, Thiamin Mononitrate (Vitamin B1) Riboflavin (Vitamin B2), Folic Acid) Eggs, Butter (Pasteurized Cream, Natural Flavorings), Sugar, Water, Dried Whey, Salt, Yeast --- Contains Allergen: Wheat --- Heating Instructions: Remove Buns from freezer and defrost in refrigerator. Serve at room temperature or toast bun for 3-5 minutes in 350-degree oven for optimal flavor. --- Net weight: 27.00 LBS. (12 ct / 12 pkgs) --- The Bonami Baking Co.

Original FDA recall reason

Undeclared milk and/or eggs from sub-ingredients and/or Contains statement.

Recall details

Recall number
H-0489-2025
Event ID
97347
FDA status
Ongoing
Initiated
Jul 24, 2025
Reported
Aug 20, 2025
Classified
Aug 13, 2025
Quantity
61,862 packages (12 dozen/package)
Location
Pittsburg, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

CA

FDA source record · H-0489-2025

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.