Food Recall Check
Class I · High risk Terminated Initiated Mar 4, 2025 (2 years ago)

Wangzhine branded Hot Pot Sauce recall

Recalled by Liaoning Cheng Da (USA) Inc · San Gabriel, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

Undeclared allergens: Soy Wheat

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Wangzhine branded Hot Pot Sauce (SPICY); Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001382

Quantity: 3420 cases

Food: Sauces, dips & dressings

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Best before: 2025-07-08

Where it was sold

California

FDA's distribution note: The firm has distributed to 5 direct account consignees here in California.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to soy, wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Liaoning Cheng Da (USA) Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 4, 2025
In FDA report of
Apr 2, 2025
Terminated
Nov 25, 2025
FDA recall number
F-0673-2025 · event 96429
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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