Kerry recalls 6-pack of 3lb KC Everyday Mac & Cheese (item #20609055) due to undeclared egg allergen. Consumers should check lot numbers 0011849964, 0011988192, 0012085206 for affected products.
“Kerry KC Everyday Mac & Cheese Recall: Undeclared Egg Allergen Risk.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/445407-kerry-kc-everyday-mac-cheese-recall-undeclared-egg-allergen-risk. Based on FDA recall #H-1237-2026.
The FDA announced on July 29, 2026, that Kerry, Inc. is recalling KC Everyday Mac & Cheese due to an undeclared egg allergen. The agency issued recall number H-1237-2026 for the Class I recall.
How to tell if you have it
Brand: Kerry
Product: KC Everyday Mac & Cheese, 3lb x 6
Item #: 20609055
Lot Numbers: 0011849964, 0011988192, 0012085206
Distribution: IA, IL, OK, SD, TX
The hazard
The product contains undeclared egg allergen. The recall is classified as Class I by the FDA.
Context
GovInfoNow's records show Kerry, Inc. has issued seven other recalls since July 11, 2016. Other recent recalls of similar products include Kerry Sun Nat HV CHDR #3 SEAS (May 3, 2024), Kerry Flour Recall (Nov. 23, 2022), and Kerry DaVinci Gourmet Caramel Sauce Recall (Nov. 20, 2019). Other recent recalls of similar products include Outside The Breadbox Bread Crumbs recall (Jan. 8, 2026), B.C. Williams Bakery Bread Mix Recall (Dec. 23, 2025), and Lunds & Byerlys Monster Cookies Recall (Dec. 3, 2025).
How to tell if you have this one
Check for the product name 'KC Everyday Mac & Cheese', 3lb x 6 pouches, and lot numbers 0011849964, 0011988192, or 0012085206. The product is fully cooked and should be kept frozen.
Brand
Kerry
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Lot Numbers
Look for lot numbers 0011849964, 0011988192, or 0012085206 on the packaging.
Where it went and when
Where it was distributed
Distributed in 5 states.
Listed by the agency
Not listed
FDA distribution: “IA, IL, OK, SD, TX” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Iowa, Oklahoma, South Dakota, Texas.
Recall timeline
FDA published this recall 14 days after the firm started it.
1Firm started the recall
2Published in FDA’s Enforcement Report
3FDA classified it Class I
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-1237-2026 (July 29, 2026)
Plain-language summary written by qwen3:4b on August 27, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.