Why it was recalled
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
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 numbers, UPCs & expiration codes
Lots: 80861; 80870; 80946; 80965
Where it was sold
Recalled product was sold to 7 distributors nationwide. Product is not for retail sale and is intended for institutional use.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- H-0150-2026
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Oct 16, 2025
- FDA report date
- Oct 29, 2025
- Quantity
- 1,040 cases across recalled products
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- M.C.I. Foods, Inc.
Original FDA data
Every field from FDA enforcement report H-0150-2026, exactly as published.
Show all FDA fields
- City
- Santa Fe Springs
- State
- CA
- Status
- Terminated
- Country
- United States
- Event ID
- 97840
- Address
- 13013 Molette St
- Code information
- Lots: 80861; 80870; 80946; 80965
- Postal code
- 90670-5521
- Report date
- Oct 29, 2025
- Product type
- Food
- Recall number
- H-0150-2026
- Classification
- Class I
- Recalling firm
- M.C.I. Foods, Inc.
- Product quantity
- 1,040 cases across recalled products
- Termination date
- Feb 18, 2026
- Reason for recall
- Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
- Voluntary / mandated
- Voluntary: Firm initiated
- 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
- Distribution pattern
- Recalled product was sold to 7 distributors nationwide. Product is not for retail sale and is intended for institutional use.
- Recall initiation date
- Oct 16, 2025
- Initial firm notification
- Letter
- Center classification date
- Oct 31, 2025