Cheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 468334 8
Summary
The FDA issued a Class I for Cheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 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-0149-2026
Action Date
2025-10-29
Status
Terminated
Category
food
Product Description
Cheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 468334 8
Lot/Code Info: Lots: 80860
Quantity Affected: 330 cases
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
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-0149-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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