PlainRecalls
FDA Food Moderate Class II Terminated

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

Reported: July 18, 2018 Initiated: May 18, 2018 #F-1618-2018

Product 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

Reason for Recall

During a FDA foreign inspection, it was found that four products did not declare allergens.

Details

Units Affected
468 boxes, all products
Distribution
One US Customer in CA
Location
Yangsan

Frequently Asked Questions

What product was recalled?
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. Recalled by Hee Chang Dairy & Food Co., LTD. Units affected: 468 boxes, all products.
Why was this product recalled?
During a FDA foreign inspection, it was found that four products did not declare allergens.
Which agency issued this recall?
This recall was issued by the FDA Food on July 18, 2018. Severity: Moderate. Recall number: F-1618-2018.