Class IITerminated in FDA datasetOct 5, 2021

Chocolate & the Chip Fluffadoodle and Fluffa-Nutta Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected

Recalling firm: Chocolate and the Chip

Why it was recalled

Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.

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The exact product

Chocolate & the Chip Fluffadoodle and Fluffa-Nutta 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%), pure vanilla extract (vanilla bean extractives in water and alcohol), Himalayan salt, baking soda (sodium bicarbonate), instant decaf coffee (decaffeinated instant coffee, caramelized sugar), CORN SYRUP, SUGAR, DEXTROSE, MODIFIED CORNSTARCH, WATER, CONTAINS LESS THAN 2% OF GELATIN, TETRASODIUM PYROPHOSPHATE (WHIPPING AID), NATURAL AND ARTIFICIAL FLAVOR, BLUE 1), 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.

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Original FDA code information

Product manufactured from July 1, 2021 to 9-30-21.

Recall details

Recall number
F-0033-2022
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

FDA source record · F-0033-2022

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.