Chocolate & the Chip Peanutbutter Spice Cookies: 4 oz / 114 grams per pack. Cookies are…
Recalling firm: Chocolate and the Chip
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 30, 2021.
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FDA code information
Product manufactured from July 1, 2021 to 9-30-21.
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Full FDA record and distribution details
Original product description
Chocolate & the Chip Peanutbutter Spice Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Ingredients: All purpose flour (bleached wheat flour, malted barley flour, niacin, reduced iron, ascorbic acid, thiamin mononitrate, riboflavin, folic acid, ascorbic acid) unsalted butter (pasteurized cream, natural flavorings), eggs, semi sweet chocolate chips (sugar, chocolate, cocoa butter, milkfat, soy lecithin, natural flavors), light brown sugar, white granulated sugar, peanut butter (Roasted peanuts 91.5% Dextrose - 6% Hydrogenated vegetable oil (rapeseed, cottonseed, soybean) - 2% Salt - .5%), cinnamon chips (Sugar, partially hydrogenated palm kernel oil, cocoa powder, natural and imitation cinnamon flavor, salt, soy lecithin, and vanillin, pure vanilla extract (vanilla bean extractives in water and alcohol), Himalayan salt, baking soda (sodium bicarbonate), instant decaf coffee (decaffeinated instant coffee, caramelized sugar), cinnamon, salt flakes. Contains: wheat, milk, eggs, soy, tree nuts (peanuts) Labels found during the inspection had undeclared wheat, milk, soy. Firm had listed ingredients on packaging but what was missing were the sub ingredients and allergen containment.
Original FDA recall reason
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Recall details
- Recall number
- F-0037-2022
- Event ID
- 88824
- FDA status
- Terminated
- Initiated
- Oct 5, 2021
- Reported
- Oct 27, 2021
- Classified
- Oct 20, 2021
- Terminated
- Nov 30, 2021
- Quantity
- 3000 units (total)
- Location
- Inglewood, CA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Press Release
Where it was distributed
Nationwide distribution
Data updated September 16, 2026. View official FDA data ↗
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