Rolling Pin brand Dubai Style Chocolate; 17.64 oz stand up pouch; Ingredients: Sugar, Cocoa Butter, Vegetable Fats, Whole Milk Powder, Pistachio (Tree Nut), Skimmed Milk Powder, Cocoa Mass, Kunefa, Soy Lecithin, Natural Vanilla Powder; Allergens: Contains Milk, Soy, Nuts (Pistachio), Gluten; Product of Belgium, Spain, USA, or Canada; Distributed & Imported by Rolling Pin Baking Company LLC; UPC # 642461215854

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Item #1932972; Distributed between May 1, 2025 and August 29, 2025
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
ROLLING PIN BAKING COMPANY LLC
Reason for Recall:
Product does not declare wheat in the allergen statement.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Rolling Pin brand Dubai Style Chocolate; 17.64 oz stand up pouch; Ingredients: Sugar, Cocoa Butter, Vegetable Fats, Whole Milk Powder, Pistachio (Tree Nut), Skimmed Milk Powder, Cocoa Mass, Kunefa, Soy Lecithin, Natural Vanilla Powder; Allergens: Contains Milk, Soy, Nuts (Pistachio), Gluten; Product of Belgium, Spain, USA, or Canada; Distributed & Imported by Rolling Pin Baking Company LLC; UPC # 642461215854

Product Codes/Lot Numbers:

Item #1932972; Distributed between May 1, 2025 and August 29, 2025

Distribution:

Distributed in: WA, OR, MT, UT, ID, CO, CA, FL, GA, AZ, NC, AL, TN, SC

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: H-0127-2026

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