Orange Jelly Sticks DARK, item number CB741-D, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declares "Ingredients: Dark Chocolate (***milk fat (butter), soya lecithin***), Sugar, Corn Syrup, Fruit Pectin,***Vegetable Oil". Manufactured By: The Candy Basket, Inc. Portland, OR.

Class I - Dangerous
Recalled: January 15, 2025 The Candy Basket Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    All lots up to 025014.
  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:
The Candy Basket Inc
Reason for Recall:
Undeclared Yellow #6, and Sodium Benzoate.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Orange Jelly Sticks DARK, item number CB741-D, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declares "Ingredients: Dark Chocolate (***milk fat (butter), soya lecithin***), Sugar, Corn Syrup, Fruit Pectin,***Vegetable Oil". Manufactured By: The Candy Basket, Inc. Portland, OR.

Product Codes/Lot Numbers:

All lots up to 025014.

Distribution:

Distributed in: CA, OR, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0556-2025

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