RECALL RECORD — CLASS IRecall closedF-0463-2016/FDA enforcement

Tonkutsu Ramen, NET WT

What you need to know

Class I
  • What happened

    Tonkutsu Ramen may contain undeclared eggs.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDAGA, IL, NJ, NYMore food

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Product identification

Source: FDA FOOD

Brand nameSun Noodle New Jersey, LLC
Recalling firmSun Noodle New Jersey, LLCTeterboro, NJ, United States
UPC / barcodes
0 85315 40003 531 143503 11501 331 150403 11507 131 151413 11517 631 152293 11526 731 152993 11532 832 143503 21501 332 150403 21507 132 151413 21517 632 152293 21526 732 152993 21532 831 143523 11501 5
Lot / date codes
  • 3114350 3115013 3115040 3115071 3115141 3115176 3115229 3115267 3115299 3115328 3214350 3215013 3215040 3215071 3215141 3215176 3215229 3215267 3215299 3215328 3114352 3115015 3115043 3115072 3115149 3115187 3115246 3115271 3115304 3115336 3214352 3215015 3215043 3215072 3215149 3215187 3215246 3215271 3215304 3215336 3114360 3115028 3115055 3115084 3115161 3115195 3115254 3115275 3115314 3214360 3215028 3215055 3215084 3215161 3215195 3215254 3215275 3215314 3115007 3115034 3115058 3115114 3115167 3115216 3115265 3115281 3115321 3215007 3215034 3215058 3215114 3215167 3215216 3215265 3215281 3215321
Distribution area
GAILNJNY

GA, IL, NJ and NY

United States

Quantity affected34, 836 units
Recall initiationFDA report date: February 10, 2016
FDA recall numberF-0463-2016

Beyond the headline

The recall, in context

Sun Noodle New Jersey, LLC initiated this food recall on December 14, 2015. The FDA enforcement report states: Tonkutsu Ramen may contain undeclared eggs. The FDA report lists distribution as: GA, IL, NJ and NY.

The FDA enforcement report describes the reason as: Tonkutsu Ramen may contain undeclared eggs.

Tonkutsu Ramen, NET WT was made or distributed by Sun Noodle New Jersey, LLC in Teterboro, NJ, United States. This page reflects FDA report F-0463-2016, dated February 10, 2016.

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, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

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 Tonkutsu Ramen, NET WT recall?

Sun Noodle New Jersey, LLC recalled Tonkutsu Ramen, NET WT in an FDA Class I enforcement action reported as F-0463-2016. Tonkutsu Ramen may contain undeclared eggs.

What are the symptoms of Undeclared allergen exposure?

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

How quickly can Undeclared allergen symptoms appear?

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

Who is most at risk from Undeclared allergen?

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

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. 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.

How do I get a refund from Sun Noodle New Jersey, LLC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0463-2016 and keep the packaging, lot code and proof of purchase if you have them.

Is the Sun Noodle New Jersey, 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-0463-2016. 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

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