Food Recall Check
Class II · Moderate risk Terminated Initiated May 16, 2024 (2 years ago)

Breadman Jalapeno Cheese Bagels recall

Recalled by Breadbox Co. · Santa Fe Springs, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Undeclared milk allergen

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Breadman Jalapeno Cheese Bagels, plastic bag, 16oz

Quantity: 130

Food: Cheese Bread & bakery

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Expiration Date - 5/21/24

Where it was sold

California

FDA's distribution note: No foreign or government consignees. The Raisin Bread and Jalapeno Cheese Bagels were distributed to 1 consignee in CA who distributes to their retail chain stores located throughout Southern CA. The Brioche products were distributed to a total of 24 restaurants within Southern CA.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Breadbox Co.
Initiated by
Voluntary: Firm initiated
Recall initiated
May 16, 2024
In FDA report of
Jul 10, 2024
Terminated
Oct 22, 2025
FDA recall number
F-1460-2024 · event 94694
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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