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