Recalls / Class II
Class IIF-0037-2022
Product
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.
- Type
- Food
- Affected lot / code info
- Product manufactured from July 1, 2021 to 9-30-21.
- Quantity
- 3000 units (total)
Why it was recalled
Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Recalling firm
- Firm
- Chocolate and the Chip
- Notification channel
- Press Release
- Type
- Voluntary: Firm initiated
- Address
- 705 Vesta St, N/A, Inglewood, California 90302-3316
Distribution
- Distribution pattern
- Nationwide distribution
Timeline
- Recall initiated
- 2021-10-05
- FDA classified
- 2021-10-20
- Posted by FDA
- 2021-10-27
- Terminated
- 2021-11-30
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0037-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings.