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Green Tea Latte; 35.3 oz. (1 kg) packet Ingredients: White sugar, Instant Whole Milk Powder (Corn Syrup, Milk cream, Lactose, Lecithin, Sodium Caseinate, Non Dairy Creamer (corn Syrup, vegetable oil, sodium caseinate, Silicon Dioxide, Skim Milk Powder, Whey Powder, Green Tea Powder, Whipped Cream Powder Citron Powder contains corn syrup 58% and Lactose 20% Imported and Distributed by: Coffee Tree USA 2203W Venice Blvd, Unit 101A Los Angeles, CA 90006 USA

Class I - Dangerous
Recalled: May 18, 2018 Hee Chang Dairy & Food Co. Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Lot 20161125; Exp date 2018.11.24
  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:

Green Tea Latte; 35.3 oz. (1 kg) packet Ingredients: White sugar, Instant Whole Milk Powder (Corn Syrup, Milk cream, Lactose, Lecithin, Sodium Caseinate, Non Dairy Creamer (corn Syrup, vegetable oil, sodium caseinate, Silicon Dioxide, Skim Milk Powder, Whey Powder, Green Tea Powder, Whipped Cream Powder Citron Powder contains corn syrup 58% and Lactose 20% Imported and Distributed by: Coffee Tree USA 2203W Venice Blvd, Unit 101A Los Angeles, CA 90006 USA

Product Codes/Lot Numbers:

Lot 20161125; Exp date 2018.11.24

Distribution:

Distributed in: US, CA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1618-2018

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