RecallHawk
Class I Recall

Wangzhine branded Hot Pot Sauce; Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001375

Liaoning Cheng Da (USA) Inc

Summary

The FDA issued a Class I for Wangzhine branded Hot Pot Sauce; Net Weight: 160 Grams, 5.64OZ; 36 units/case; by Liaoning Cheng Da (USA) Inc. Reason: (Imported) Hot Pot Sauce contains undeclared allergens (Wheat and Soy).

Details

Source

Food Recall

External ID

F-0672-2025

Action Date

2025-04-02

Status

Terminated

Category

food

Product Description

Wangzhine branded Hot Pot Sauce; Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001375

Lot/Code Info: Best before: 2026-07-02

Quantity Affected: 3650 cases

Reason for Recall

(Imported) Hot Pot Sauce contains undeclared allergens (Wheat and Soy)

Distribution

The firm has distributed to 5 direct account consignees here in California.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-03-04

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Liaoning Cheng Da (USA) Inc has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Liaoning Cheng Da (USA) Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Liaoning Cheng Da (USA) Inc have FDA actions?

Liaoning Cheng Da (USA) Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0672-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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