Black Bean Cereal Latte; 28.2 oz. package Ingredients: Non Dairy Creamer (corn syrup, vegetable oil, Sodium Caseinate, Silicon dioxide), Rice Powder, Bean Powder, Silicon dioxide, Refined Salt, Black Sesame. Corn syrup 57% Hydrogenated coconut oil 28% Sweet whey powder 10% (the firm said this is 100% pure whey/milk ingredient) Sodium caseinate 1.3%. Imported and Distributed by: Coffee Tree USA 2203W Venice Blvd, Unit 101A Los Angeles, CA 90006 USA

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot 20170206; Exp date 2018.08.05
  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:
Hee Chang Dairy & Food Co., LTD
Reason for Recall:
During a FDA foreign inspection, it was found that four products did not declare allergens.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Black Bean Cereal Latte; 28.2 oz. package Ingredients: Non Dairy Creamer (corn syrup, vegetable oil, Sodium Caseinate, Silicon dioxide), Rice Powder, Bean Powder, Silicon dioxide, Refined Salt, Black Sesame. Corn syrup 57% Hydrogenated coconut oil 28% Sweet whey powder 10% (the firm said this is 100% pure whey/milk ingredient) Sodium caseinate 1.3%. Imported and Distributed by: Coffee Tree USA 2203W Venice Blvd, Unit 101A Los Angeles, CA 90006 USA

Product Codes/Lot Numbers:

Lot 20170206; Exp date 2018.08.05

Distribution:

Distributed in: US, CA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1615-2018

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