Green Tea Latte (Hee Chang) - Undeclared Allergens (2018)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Hee Chang Dairy & Food Co., LTD
Lot Codes / Batch Numbers
Lot 20161125, Exp date 2018.11.24
Products Sold
Lot 20161125; Exp date 2018.11.24
Hee Chang Dairy & Food Co., LTD is recalling Green Tea Latte; 35.3 oz. (1 kg) packet Ingredients: White sugar, Instant Whole Milk Powder (Corn due to During a FDA foreign inspection, it was found that four products did not declare allergens.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
During a FDA foreign inspection, it was found that four products did not declare allergens.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, IN
Page updated: Jan 6, 2026