Drug Emporium Yogurt Flavored Pretzels, 8oz (227g) , GNS Foods, Arlington, TX 76011
Summary
The FDA issued a Class II for Drug Emporium Yogurt Flavored Pretzels, 8oz (227g) , GNS Foods, Arlington, TX 76 by GNS Foods, Inc. Reason: A recall of lactose or lactose powder from Grande Ingredients in Wisconsin. The ingredient has the potential to be contaminated with Salmonella.
Details
Source
Food Recall
External ID
F-1456-2024
Action Date
2024-07-10
Status
Terminated
Category
food
Product Description
Drug Emporium Yogurt Flavored Pretzels, 8oz (227g) , GNS Foods, Arlington, TX 76011
Lot/Code Info: Lot Number or ID: 30723, Expiration/Use By Date: 2025-01-22
Quantity Affected: 96 bags
Reason for Recall
A recall of lactose or lactose powder from Grande Ingredients in Wisconsin. The ingredient has the potential to be contaminated with Salmonella
Distribution
Texas, Louisiana
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-06
Company
Arlington, TX
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 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (GNS Foods, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GNS Foods, Inc have FDA actions?
This is the only FDA action we have on record for GNS Foods, Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1456-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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