RecallHawk
Class I Recall

Lay s Classic Party Size Potato Chips 13 oz. (368.5 g) UPC 028400310413 packaged in a yellow flexible bag and Lay s Clas

Frito-Lay, Inc. Headquarters

Summary

The FDA issued a Class I for Lay s Classic Party Size Potato Chips 13 oz. (368.5 g) UPC 028400310413 packaged by Frito-Lay, Inc. Headquarters. Reason: Undeclared milk.

Details

Source

Food Recall

External ID

F-0925-2023

Action Date

2023-05-31

Status

Terminated

Category

food

Product Description

Lay s Classic Party Size Potato Chips 13 oz. (368.5 g) UPC 028400310413 packaged in a yellow flexible bag and Lay s Classic Mix and Match Potato Chips 15 5/8 oz (442.9 g) UPC 0028400720151 packaged in a yellow flexible bag

Lot/Code Info: Must have both Guaranteed Fresh 18 Jul 2023 766310622 And any one of these Manufacturing Codes 105 04:55 105 04:56 105 04:57 105 04:58 105 04:59 105 05:00 105 05:01 105 05:02; Must have both Guaranteed Fresh 18 Jul 2023 766310618 And any one of these Manufacturing Codes 105 04:55 105 04:56 105 04:57 105 04:58 105 04:59 105 05:00 105 05:01 105 05:02

Quantity Affected: 200 bags

Reason for Recall

Undeclared milk

Distribution

Connecticut, Massachusetts, Maine and New Hampshire

Type: Voluntary: Firm initiated

Recall Initiated: 2023-05-04

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 71 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 I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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-0925-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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