RecallHawk
Class I Recall

Gelson's Sea Salt Pretzels, 4.5oz poly bags, UPC: 23631-11185, 12 pack

Dakota Style, Inc

Summary

The FDA issued a Class I for Gelson's Sea Salt Pretzels, 4.5oz poly bags, UPC: 23631-11185, 12 pack by Dakota Style, Inc. Reason: May contain undeclared milk.

Details

Source

Food Recall

External ID

F-1244-2023

Action Date

2023-07-19

Status

Terminated

Category

food

Product Description

Gelson's Sea Salt Pretzels, 4.5oz poly bags, UPC: 23631-11185, 12 pack

Lot/Code Info: D2222022 Best by 8/11/2023; D2482022 Best by 9/29/2023; D0592023 Best by 04/13/2024

Quantity Affected: 334,357 total bags

Reason for Recall

May contain undeclared milk

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2023-04-13

Company

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

Dakota Style, Inc has 4 FDA actions in our database, including 4 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 (Dakota Style, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Dakota Style, Inc have FDA actions?

Dakota Style, Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1244-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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