Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported December 24, 2014
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
Firm was notified by CFIA and FDA that CFIA testing found undeclared milk allergen in the product.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
Evershing International Trading Inc. recalled Wake-Up Instant Coffee Mix (weasel coffee) Melange de Cafe Instantane Ca Phe Hoa Tan (h… - a critical-severity action.
Wake-Up Instant Coffee Mix (weasel coffee) Melange de Cafe Instantane Ca Phe Hoa Tan (h… was recalled by Evershing International Trading Inc. in December 24, 2014. Reason: Firm was notified by CFIA and FDA that CFIA testing found undeclared milk allergen in the product.. Check the official notice for the remedy. Verify recall #F-0727-2015 with the FDA Food before acting.
The recall
Evershing International Trading Inc. issued this critical-severity FDA Food recall-Firm was notified by CFIA and FDA that CFIA testing found undeclared milk allergen in the product..
- Critical
- severity level
- Class I
- classification
- December 24, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0727-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0727-2015) was formally reported on December 24, 2014, with the manufacturer initiating the action on November 20, 2014. It is classified under Critical severity (Class I), with a current status of Terminated. Evershing International Trading Inc. is listed as the recalling firm, operating out of San Jose, CA. Federal records list the affected scope as 5949.00 cases of product 521509; 2225.00 cases of product 521510.
The documented reason for this recall is: Firm was notified by CFIA and FDA that CFIA testing found undeclared milk allergen in the product. Distribution data in the federal record shows the product reached: CA, WA, OR, OK, AZ. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
5949.00 cases of product 521509; 2225.00 cases of product 521510
Related Recalls
6
2 from same agency
Product description
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 Industry Zone, An Binh Ward, Bien Hoa City, Dong Nai Province.
Reason for recall
Firm was notified by CFIA and FDA that CFIA testing found undeclared milk allergen in the product.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-0727-2015 |
| Date reported | December 24, 2014 |
| Date initiated | November 20, 2014 |
| Recalling firm | Evershing International Trading Inc. |
| Firm location | San Jose, CA |
| Affected scope | 5949.00 cases of product 521509; 2225.00 cases of product 521510 |
| Distribution | CA, WA, OR, OK, AZ |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0727-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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 Industry Zone, An Binh Ward, Bien Hoa City, Dong Nai Province.. Recalled by Evershing International Trading Inc.. Units affected: 5949.00 cases of product 521509; 2225.00 cases of product 521510.
Why was this product recalled? ▼
Firm was notified by CFIA and FDA that CFIA testing found undeclared milk allergen in the product.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on December 24, 2014. Severity: Critical. Recall number: F-0727-2015.
Where was the recalled product distributed? ▼
Distribution: CA, WA, OR, OK, AZ.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0727-2015) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported December 24, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.