RecallHawk
Class III Recall

Rold Gold Original Classic Tiny Twists Pretzels in 16oz UPC 2840004768 packaged in a flexible bag

Frito-Lay, Inc. Headquarters

Summary

The FDA issued a Class III for Rold Gold Original Classic Tiny Twists Pretzels in 16oz UPC 2840004768 packaged by Frito-Lay, Inc. Headquarters. Reason: Undeclared soy lecithin.

Details

Source

Food Recall

External ID

F-0652-2023

Action Date

2023-04-05

Status

Terminated

Category

food

Product Description

Rold Gold Original Classic Tiny Twists Pretzels in 16oz UPC 2840004768 packaged in a flexible bag

Lot/Code Info: Both Guaranteed Fresh date of 20 JUN 2023 And one of these 9-digit Manufacturing Codes 232205928, 332306028, 332106028, 332206028, 432306128, 232205927, 332306027, 332106027, 332206027, 432306127

Quantity Affected: 888 bags

Reason for Recall

Undeclared soy lecithin

Distribution

GA, AL, MS, LA, FL

Type: Voluntary: Firm initiated

Recall Initiated: 2023-03-06

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 66 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 III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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-0652-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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