RecallHawk
Class II Recall

16 oz. bags of Trader Joe's Organic Yellow Tortilla Chip Rounds. UPC: 0074-0449 Distributed and Sold exclusively by:

Snak King Corporation

Summary

The FDA issued a Class II for 16 oz. bags of Trader Joe's Organic Yellow Tortilla Chip Rounds. UPC: 0074-044 by Snak King Corporation. Reason: Bags of Trader Joe's Organic Round Tortilla Chips were found to contain small amounts of Trader Joes Spicy Cheese Crunchies which includes the allerge.

Details

Source

Food Recall

External ID

F-0047-2023

Action Date

2022-10-26

Status

Terminated

Category

food

Product Description

16 oz. bags of Trader Joe's Organic Yellow Tortilla Chip Rounds. UPC: 0074-0449 Distributed and Sold exclusively by: Trader Joe's, Monrovia, CA 91016 Distributed and sold exclusively by: Trader Joe's, Monrovia, CA 91016 Distributed and Sold Exclusively By: Trader Joe's, Monrovia, CA 91016

Lot/Code Info: Sell By dates 01/18/23, 01/19/23, 01/20/23

Quantity Affected: 14,412 cases

Reason for Recall

Bags of Trader Joe's Organic Round Tortilla Chips were found to contain small amounts of Trader Joes Spicy Cheese Crunchies which includes the allergens of milk and soy which are not declared on the label.

Distribution

Affected product was distributed to the following states: AL, AR, AZ, CA, CO, ID, KS, LA, NM, NV,OK, OR, TN, TX, UT, WA

Type: Voluntary: Firm initiated

Recall Initiated: 2022-09-29

Company

Snak King Corporation

City Of Industry, CA

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 41 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Snak King Corporation has 2 FDA actions in our database, including 2 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 (Snak King Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Snak King Corporation have FDA actions?

Snak King Corporation has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0047-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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