Liaoning Cheng Da (USA) Inc food recall: Wangzhine branded Hot Pot Sauce
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 96429
- Recall initiated
- Mar 4, 2025
- Classified by FDA
- Mar 27, 2025
- Posted in Enforcement Report
- Apr 2, 2025
- Terminated
- Nov 25, 2025
- Recalling firm
- Liaoning Cheng Da (USA) Inc
- Firm location
- San Gabriel, CA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 2
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
(Imported) Hot Pot Sauce contains undeclared allergens (Wheat and Soy)
(Imported) Hot Pot Sauce (SPICY) contains undeclared allergens (Wheat and Soy)
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Mar 4, 2025. FDA classified it 23 days later, on Mar 27, 2025. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: The firm has distributed to 5 direct account consignees here in California.
Recalled products (2)
F-0672-2025 Class I Terminated
Wangzhine branded Hot Pot Sauce; Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001375
Codes / lots: Best before: 2026-07-02
Quantity: 3650 cases
F-0673-2025 Class I Terminated
Wangzhine branded Hot Pot Sauce (SPICY); Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001382
Codes / lots: Best before: 2025-07-08
Quantity: 3420 cases
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 96429
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.