FDA recall record

Best Express Foods Universal Bakery Organic Sunrise Energy Bars 32 oz recall — FDA F-1491-2024

Potential undeclared gluten product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.

Class IIclassification
F-1491-2024official record ID
Jul 31, 2024report date

Recall record at a glance

Official recordF-1491-2024
CategoryFood Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBest Express Foods, Inc.
Report dateJul 31, 2024
Recall initiation dateJun 18, 2024
Quantity104,160 units
LocationStockton, CA, United States

Official product description

Universal Bakery Organic Sunrise Energy Bars 32 oz. and 10 oz. Gluten Free USDA Organic Made With: Rolled Oats, Dried Fruits, Flax Seeds, Quinoa, Coconut, Pumpkin Seeds, Chia Seeds + More Ingredients: Organic Rolled Oats, Organic Sunflower Oil, Organic Evaporated Cane Juice, Organic Tapioca Syrup, Organic Dried Apples, Organic Dried Cranberries, Organic Raisins, Organic Tapioca Flour, Organic Quinoa, Organic Sunflower Seeds, Organic Flax Seeds, Organic Flax Meal, Organic Shredded Coconut, Organic Oat Flour, Organic Pumpkin Seeds, Organic Olive Oil, Organic Sugar, Organic Chia Seeds, Organic Cashews, Organic Cinnamon, Vanilla Extract, Sea Salt, Baking Soda. ALLERGY INFORMATION: This Product Contains Coconut and Tree Nuts. Produced in a facility that may contain Wheat, Soy, Eggs, Peanuts and Tree Nuts. Best Express Foods, Inc. Stockton, CA 95206 USA Comments and Questions: 1-800-282-6645 cs@bestexpressfoods.com www.bestxfoods.com Certified Organic By CCOF Made in California

Why the product was recalled

Potential undeclared gluten product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.

Distribution information

U.S. distribution to the following: CA, CO, AZ, WA, UT, TX, NJ, MD, IL, MI, MN, GA, FL Foreign distribution to the following: Canada

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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