RecallHawk
Class II Recall

12/5 oz. bags of O-Organic Sea Salt Popcorn. UPC Code: 79893403038

Snak King Corporation

Summary

The FDA issued a Class II for 12/5 oz. bags of O-Organic Sea Salt Popcorn. UPC Code: 79893403038 by Snak King Corporation. Reason: A potato stick snack with a milk allergen was found in the O-Organic Sea Salt Popcorn line's recycle chute..

Details

Source

Food Recall

External ID

F-1050-2022

Action Date

2022-05-18

Status

Terminated

Category

food

Product Description

12/5 oz. bags of O-Organic Sea Salt Popcorn. UPC Code: 79893403038

Lot/Code Info: Lot numbers: 8124905, 80125929, 8125929, 8124905, 8125929 ; Best buy dates 09/24/2022 and 09/25/2022.

Quantity Affected: 4832 cases

Reason for Recall

A potato stick snack with a milk allergen was found in the O-Organic Sea Salt Popcorn line's recycle chute.

Distribution

Connecticut, Delaware, Maryland, New Jersey, New York, Pennsylvania, Virginia, Washington DC, Illinois, Indiana, Iowa, California, Hawaii, Nevada, Oregon, Washington, Alaska, and Idaho.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-09

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 29 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-1050-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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