Frito-Lay recalls Chickpea Veggie Crisps (UPC 02840020646) due to undeclared milk allergen. Consumers should check product codes and contact Frito-Lay for details.
“Frito-Lay Chickpea Veggie Crisps Recall: Undeclared Milk Allergen Hazard.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/10152-frito-lay-chickpea-veggie-crisps-recall-undeclared-milk-allergen-hazard. Based on FDA recall #F-0470-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0470-2024%22&limit=1).
The FDA announced on Nov. 8, 2023, that Frito-Lay, Inc. Headquarters voluntarily recalled Chickpea Veggie Crisps due to undeclared milk allergens. Owners should contact the company for a refund.
How to tell if you have it
Frito-Lay Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646
Lot codes: 55432514MH, 55432516MH, 55432517MH
The hazard
The product poses a risk to individuals with milk allergies because it contains undeclared milk. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Frito-Lay, Inc. Headquarters has had 9 other recalls on record since Jan. 21, 2021. Other recent recalls of similar products include Frito-Lay Tostitos Cantina Yellow Corn Chips Recall (March 26, 2025), Pearl Milling Pancake Mix Recall (Jan. 14, 2025), and Frito-Lay Doritos Nacho Cheese Chips Recall (July 18, 2023).
How to tell if you have this one
Check for the UPC 02840020646 or product codes 55432514MH, 55432516MH, 55432517MH. The product is sold in 6 1/4 oz bags.
Brand
Frito-Lay
Product
Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Codes
Look for the UPC 02840020646 or product codes 55432514MH, 55432516MH, 55432517MH on the packaging.
Where it went and when
Where it was distributed
Distributed in 26 states.
Listed by the agency
Not listed
FDA distribution: “The product covered by this recall was distributed to retail stores in the following states, as well as e-commerce customers: Alabama, Arkansas, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Missouri,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arkansas, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Missouri, Nebraska, New Hampshire, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Texas, Virginia, West Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 12 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
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 #F-0470-2024 (November 8, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0470-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.