RecallHawk
Class II Recall

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

Frito-Lay, Inc. Headquarters

Summary

The FDA issued a Class II for Doritos Nacho Cheese Flavored Tortilla Chips Party Size-14 1/2 oz. (411 g) Dorit by Frito-Lay, Inc. Headquarters. Reason: Potential to contain undeclared soy & wheat ingredients..

Details

Source

Food Recall

External ID

F-1458-2023

Action Date

2023-08-30

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: 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

Quantity Affected: 6,642 bags

Reason for Recall

Potential to contain undeclared soy & wheat ingredients.

Distribution

PA

Type: Voluntary: Firm initiated

Recall Initiated: 2023-07-18

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frito-Lay, Inc. Headquarters has 8 FDA actions in our database, including 8 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Frito-Lay, Inc. Headquarters) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Frito-Lay, Inc. Headquarters have FDA actions?

Frito-Lay, Inc. Headquarters has 8 FDA actions in our database, including 8 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1458-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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