DA CHENG VEGETARIAN FOOD INC. Recall: Vegan Golden Nuggets were sampled by the FDA and found to contain egg that is not declared on the label.

🇺🇸 United States

1. October 14, 2022 - Recall initiated
2. November 16, 2022 - Reported by source
3. January 24, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0138-2023

Event ID

90994

Status

Terminated

Classification

Class I

Company

DA CHENG VEGETARIAN FOOD INC.

Product description

Vegan Golden Nuggets, (6.6 lb bags) Ingredients: (NON GMO) Textured Soybean Fiber, Isolated Soy Protein, Soybean Oil, Sugar, Salt, Pepper, Vegan Chicken Flavor Seasoning (Food Additive: Modified Starch Seasoning, Yeast Extract (Yeast Extract, Salt, Water), Crisp Powder, Bread Powder (Wheat). Keep Frozen

Quantity

2 cases, 6 bags per case

Reason

Vegan Golden Nuggets were sampled by the FDA and found to contain egg that is not declared on the label.

Recall initiation date

October 14, 2022

Report date

November 16, 2022

Classification date

Not published in this source record

Termination date

January 24, 2023

Distribution pattern

Product was distributed in Utah, Virginia, Texas, and California. Mostly distributed to restaurants, one distributor in Houston, Texas, one retail store in Orange County in Southern California.

UPC, lot, and code information

Expiration Dates between 2023-09-22 and 2024-01-11 are implicated in this recall Code: L175

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 90994 with 2 other product entries in Public Health Trace.

Responsible company: DA CHENG VEGETARIAN FOOD INC.

Other recalls from DA CHENG VEGETARIAN FOOD INC.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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