Food Recall Check
Class II · Moderate risk Terminated Initiated Jul 18, 2023 (3 years ago)

Doritos Nacho Cheese Flavored Tortilla Chips Party Size-14 recall

Recalled by Frito-Lay, Inc. Headquarters · Plano, TX, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Potential to contain undeclared soy & wheat ingredients.

Undeclared allergens: Soy Wheat

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Doritos Nacho Cheese Flavored Tortilla Chips Party Size-14 1/2 oz. (411 g) Doritos Nacho Cheese Flavored Tortilla Chips, 1 oz.

Quantity: 6,642 bags

Food: Cheese Chips & snacks Bread & bakery

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

UPC-0 28400 51779 9 Guaranteed Fresh Date Of 26 Sept 2023 Manufacturing Codes/Time Stamps 465218037 X 22:47 22:59 465218137 X 23:00 23:06 UPC-0 28400 09089 6 Guaranteed Fresh Date Of 26 Sept 2023 Manufacturing Codes/Time Stamps 465218034 X 22:47 - 22:54

Where it was sold

Pennsylvania

FDA's distribution note: PA

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy, wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Frito-Lay, Inc. Headquarters
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 18, 2023
In FDA report of
Aug 30, 2023
Terminated
Apr 10, 2024
FDA recall number
F-1458-2023 · event 92731
Official record
FDA enforcement report search

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