FDA recall record
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 i...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of March 16, 2015. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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. 6 oz) 17g in Plastic Bag 2. 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 Industry Zone, An Binh Ward, Bien Hoa City, Dong Nai Province.
Reason
Firm was notified by CFIA and FDA that CFIA testing found undeclared milk allergen in the product.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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. 6 oz) 17g in Plastic Bag 2. 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 Industry Zone, An Binh Ward, Bien Hoa City, Dong Nai Province.
Code information listed by FDA
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
Distribution and firm information
Recalling firm listed by FDA: Evershing International Trading Inc.
Firm location listed by FDA: San Jose, CA, United States
Distribution reported by FDA: CA, WA, OR, OK, AZ
Product quantity listed by FDA: 5949.00 cases of product 521509; 2225.00 cases of product 521510
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.