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RECALL RECORD — CLASS IRecall closedF-0209-2021/FDA enforcement
Gh Foods Ca LLC·Food·Dec 22, 2020

Asian Noodle Salad Kit 2/5 lb

What you need to know

Class I

  • What happened

    Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDACA, CO, DC, INMore food

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Product identification

Source: FDA FOOD

Brand nameGh Foods Ca LLC
Recalling firmGh Foods Ca LLCSacramento, CA, United States
UPC / barcodes
8 26767 00000 020 826766 84002 5
Lot / date codes
  • Best by dates from: Amazon- December 12-23, 2020
  • Whole Foods - December 12, 2020 to January 2, 2021
Distribution area
CACODCIN

Whole Foods distribution to CA and CO DC's. 6 Amazon stores in CA.

United States

Quantity affected87 cases - 2 x 5 lb. per case
Recall initiationFDA report date: January 27, 2021
FDA recall numberF-0209-2021

Beyond the headline

The recall, in context

Gh Foods Ca LLC initiated this food recall on December 22, 2020. The FDA enforcement report states: Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,. The FDA report lists distribution as: Whole Foods distribution to CA and CO DC's. 6 Amazon stores in CA.

The FDA enforcement report describes the reason as: Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,

Asian Noodle Salad Kit 2/5 lb was made or distributed by Gh Foods Ca LLC in Sacramento, CA, United States. This page reflects FDA report F-0209-2021, dated January 27, 2021.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared allergen

Symptoms to watch for

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

When symptoms may appear

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Higher-risk groups

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What to do now

  1. 1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
  2. 2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Asian Noodle Salad Kit 2/5 lb recall?

Gh Foods Ca LLC recalled Asian Noodle Salad Kit 2/5 lb in an FDA Class I enforcement action reported as F-0209-2021. Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

Is the Gh Foods Ca LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0209-2021. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Gh Foods Ca LLC

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Gh Foods Ca LLC

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Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,

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Gh Foods Ca LLC

Spinach and Orzo Pasta Kit 2/5 lb

Contain Eggs was not listed on scale label printed at retail stores. Label does state that the product May contain any of the eight allergen that are listed out on the label,

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.