The Granola Bar brand The OG Bar; 4 oz; Ingredients: Oats, brown sugar, honey, almonds, butter, olive oil, cashews, coco
Summary
The FDA issued a Class II for The Granola Bar brand The OG Bar; 4 oz; Ingredients: Oats, brown sugar, honey, a by The Granola Bar. Reason: Product contains undeclared milk and soy..
Details
Source
Food Recall
External ID
F-0421-2025
Action Date
2025-01-29
Status
Terminated
Category
food
Product Description
The Granola Bar brand The OG Bar; 4 oz; Ingredients: Oats, brown sugar, honey, almonds, butter, olive oil, cashews, coconut flakes, chia seeds, vanilla extract, kosher salt; Contains: Tree nuts. Baked in a facility that also processes wheat, eggs, dairy, soy and nuts.
Lot/Code Info: No codes.
Quantity Affected: 25 units
Reason for Recall
Product contains undeclared milk and soy.
Distribution
CT, NY
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-31
Company
Westport, CT
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 36 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 (The Granola Bar) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Granola Bar have FDA actions?
This is the only FDA action we have on record for The Granola Bar in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0421-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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