RecallHawk
Class II Recall

Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646

Frito-Lay, Inc. Headquarters

Summary

The FDA issued a Class II for Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646 by Frito-Lay, Inc. Headquarters. Reason: Undeclared Milk Allergen.

Details

Source

Food Recall

External ID

F-0470-2024

Action Date

2023-12-06

Status

Terminated

Category

food

Product Description

Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646

Lot/Code Info: 55432514MH 55432516MH 55432517MH

Quantity Affected: 16100 bags

Reason for Recall

Undeclared Milk Allergen

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, Nebraska, New Hampshire, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Texas, Virginia, West Virginia and Wisconsin.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-11-08

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 18 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-0470-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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