RecallHawk
Class II Recall

Breadman Jalapeno Cheese Bagels, plastic bag, 16oz

Breadbox Co.

Summary

The FDA issued a Class II for Breadman Jalapeno Cheese Bagels, plastic bag, 16oz by Breadbox Co.. Reason: Undeclared milk allergen.

Details

Source

Food Recall

External ID

F-1460-2024

Action Date

2024-07-10

Status

Terminated

Category

food

Product Description

Breadman Jalapeno Cheese Bagels, plastic bag, 16oz

Lot/Code Info: Expiration Date - 5/21/24

Quantity Affected: 130

Reason for Recall

Undeclared milk allergen

Distribution

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.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-16

Company

Breadbox Co.

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 51 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 "F-1460-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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