Wake-Up Instant Coffee Mix (Evershing) – undeclared milk (2014)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
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
Wake-Up Instant Coffee Mix (weasel coffee) Melange de Cafe Instantane Ca Phe Hoa Tan (huong caon) 3 in one; sold in two packing configurations: 1. 20 bags x (0.6 oz) 17g in Plastic Bag 2. 18 bags x (0.6 oz) 17g in Paper Box. Original ingredient statement: Non-Dairy Creamer, Sugar, instant Coffee, Maltodextrin, Caramel (150A) salt, flavor. Sole distributor in USA: Evershing International Trading, San Jose, CA: Manufactured by : Vinacafe Bien Hoa Joinstock Company Bien Hoa 1 Indu
Brand
Evershing International Trading Inc.
Lot Codes / Batch Numbers
Plastic Bags: Product code 521510, Lot D19, Expire: 07-2016, UPC Code: 8934683002780 Carton: Product Code 521509, Lot E01, Expire: 07-2016, UPC Code: 8934683008478
Products Sold
Plastic Bags: Product code 521510; Lot D19, Expire: 07-2016, UPC Code: 8934683002780 Carton: Product Code 521509; Lot E01, Expire: 07-2016, UPC Code: 8934683008478
Evershing International Trading Inc. is recalling Wake-Up Instant Coffee Mix (weasel coffee) Melange de Cafe Instantane Ca Phe Hoa Tan (huong caon) due to Firm was notified by CFIA and FDA that CFIA testing found undeclared milk allergen in the product.. 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
Firm was notified by CFIA and FDA that CFIA testing found undeclared milk allergen in the product.
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
AZ, CA, OK, OR, WA
Page updated: Jan 6, 2026