RecallHawk
Class I Recall

Tostitos Avocado Salsa Jar Dip 15 oz, UPC 2840005597 packaged in a clear glass jar

Frito-Lay, Inc. Headquarters

Summary

The FDA issued a Class I for Tostitos Avocado Salsa Jar Dip 15 oz, UPC 2840005597 packaged in a clear glass j by Frito-Lay, Inc. Headquarters. Reason: Undeclared milk.

Details

Source

Food Recall

External ID

F-1251-2023

Action Date

2023-07-26

Status

Terminated

Category

food

Product Description

Tostitos Avocado Salsa Jar Dip 15 oz, UPC 2840005597 packaged in a clear glass jar

Lot/Code Info: BB dates: Located on upper rim of jar: 2 NOV 23 OR 3 NOV 23

Quantity Affected: 100,980 jars

Reason for Recall

Undeclared milk

Distribution

All 50 states - Direct to retail locations Customer List attached

Type: Voluntary: Firm initiated

Recall Initiated: 2023-06-16

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 61 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-1251-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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