Recall Radar

Disclaimer: Recall Radar is an informational summary of public FDA enforcement reports. It is not medical advice. Always confirm details with the FDA, the company, a pharmacist, or a doctor before making health decisions.

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Class IIDietary supplement

Pumpkin Spice No Bake Cookie recall

Summary

Best Friends Bakery, LLC is recalling PUMPKIN SPICE NO BAKE COOKIE NET WT 3.5 oz. INGREDIENTS (dietary supplement). According to the FDA report, the reason is: Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product. The FDA rated this a Class II: the product may cause temporary or medically reversible health problems; serious harm is unlikely. Recall status: Ongoing.

Details from the FDA report

Product
PUMPKIN SPICE NO BAKE COOKIE NET WT 3.5 oz. INGREDIENTS: WHOLE GRAIN OATS, MILK, MARGARINE***WATER, SALT, CONTAINS LESS THAN 2% OF THE FOLLOWING: SOY LECITHIN, VEGETABLE MONO & DIGLYCERIDES, POTASSIUM SORBATE***, CITRIC ACID, NATURAL & ARTIFICIAL FLAVOR, BETA CAROTENE, VITAMIN A PALMITATE ADDED, PEANUT BUTTER***VANILLA***PUMPKIN PIE SPICE***GLYCERINE, PAPRIKA OLEORESINM, POTASSIUM SORBATE CONTAINS: EGG, MILK, SOY, WHEAT MADE IN A FACILITY WITH PEANUTS AND TREE NUTS UPC 8 10158 14087 5 Michelle's Bakery 101 Fashion Ave Connelly Springs, NC 28612
Reason
Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product.
Lot / code info
Lot 20326
Quantity
1,416/3.5oz cookies
Distribution
Product was shipped to the following states: AL, FL, GA, IN, KY, MI, OH, TN, VA & WV.
Recalling company
Best Friends Bakery, LLC, Connelly Springs, NC United States
Recall started
August 17, 2026
FDA report date
September 23, 2026
Classification
Class II: The product may cause temporary or medically reversible health problems; serious harm is unlikely.
Voluntary / mandated
Voluntary: Firm initiated
Status
Ongoing
Recall number
H-1386-2026

What to do

View the FDA source record (openFDA) · FDA recalls page

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