RecallHawk
Class I Recall

Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.5

M.C.I. Foods, Inc.

Summary

The FDA issued a Class I for Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 by M.C.I. Foods, Inc.. Reason: Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes.

Details

Source

Food Recall

External ID

H-0150-2026

Action Date

2025-10-29

Status

Terminated

Category

food

Product Description

Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.50 oz; 72 count/case; UPC# 1 070657 497861 1

Lot/Code Info: Lots: 80861; 80870; 80946; 80965

Quantity Affected: 1,040 cases across recalled products

Reason for Recall

Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes

Distribution

Recalled product was sold to 7 distributors nationwide. Product is not for retail sale and is intended for institutional use.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-10-16

Company

M.C.I. Foods, Inc.

Santa Fe Springs, CA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 91 food recalls issued in the same week, part of 204 food-related FDA actions this month.

M.C.I. Foods, Inc. has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (M.C.I. Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does M.C.I. Foods, Inc. have FDA actions?

M.C.I. Foods, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0150-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions