RECALL RECORD — CLASS IIRecall closedF-0724-2017/FDA enforcement

You-ka Fresh Ramune NET WT

What you need to know

Class II
  • What happened

    JFC International is recalling Fizzy Candy Punch Ramune because it may contain undeclared wheat allergen.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 FDACA, CT, MA, NJ +1 moreMore food

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Product identification

Source: FDA FOOD

Brand nameJ F C International INC
Recalling firmJ F C International INCLos Angeles, CA, United States
UPC / barcodes
4 902486 11106 4
Lot / date codes
  • JAN CODE: 4 902486 111064 Best By 2017.11.15 or before
Distribution area
CACTMANJNY

CA, CT, MA, NJ, and NY

United States

Quantity affected391 packs
Recall initiationFDA report date: December 21, 2016
FDA recall numberF-0724-2017

Beyond the headline

The recall, in context

J F C International INC initiated this food recall on November 23, 2016. The FDA enforcement report states: JFC International is recalling Fizzy Candy Punch Ramune because it may contain undeclared wheat allergen. The FDA report lists distribution as: CA, CT, MA, NJ, and NY.

The FDA enforcement report describes the reason as: JFC International is recalling Fizzy Candy Punch Ramune because it may contain undeclared wheat allergen.

You-ka Fresh Ramune NET WT was made or distributed by J F C International INC in Los Angeles, CA, United States. This page reflects FDA report F-0724-2017, dated December 21, 2016.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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 wheat or gluten

Symptoms to watch for

Wheat allergy can cause hives, nausea, cramps, breathing difficulty or anaphylaxis. For celiac disease, even small amounts of gluten can cause intestinal damage.

When symptoms may appear

Allergic reactions can begin within minutes to hours. Celiac-related intestinal effects may be delayed.

Higher-risk groups

People with wheat allergy, celiac disease, non-celiac gluten sensitivity or a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a wheat allergy or must avoid gluten.
  2. 2Seek emergency care for breathing difficulty or other signs of a severe allergic reaction.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

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 You-ka Fresh Ramune NET WT recall?

J F C International INC recalled You-ka Fresh Ramune NET WT in an FDA Class II enforcement action reported as F-0724-2017. JFC International is recalling Fizzy Candy Punch Ramune because it may contain undeclared wheat allergen.

What are the symptoms of Undeclared wheat or gluten exposure?

Wheat allergy can cause hives, nausea, cramps, breathing difficulty or anaphylaxis. For celiac disease, even small amounts of gluten can cause intestinal damage.

How quickly can Undeclared wheat or gluten symptoms appear?

Allergic reactions can begin within minutes to hours. Celiac-related intestinal effects may be delayed.

Who is most at risk from Undeclared wheat or gluten?

People with wheat allergy, celiac disease, non-celiac gluten sensitivity or a history of anaphylaxis.

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 the product if you have a wheat allergy or must avoid gluten. Seek emergency care for breathing difficulty or other signs of a severe allergic reaction. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from J F C International INC?

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-0724-2017 and keep the packaging, lot code and proof of purchase if you have them.

Is the J F C International INC 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-0724-2017. 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.