ACTIVE RECALL — CLASS IIIActive recallH-0127-2027/FDA enforcement

Jovy Watermelon Gummy Rings

What you need to know

Class III
  • What happened

    Undeclared allergen ingredient (Red#40)

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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.

Active recall · classified by the FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameEl Ruisenor De Mexico, INC.
Recalling firmEl Ruisenor De Mexico, INC.Vernon, CA, United States
UPC / barcodes
7 12199 08351 0
Lot / date codes
  • Lot: 6101
Distribution area
IN

Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

United States

Quantity affected1, 395 pounds
Recall initiationFDA report date: October 28, 2026
FDA recall numberH-0127-2027

Beyond the headline

The recall, in context

El Ruisenor De Mexico, INC. initiated this food recall on August 24, 2026. The FDA enforcement report states: Undeclared allergen ingredient (Red#40). The FDA report lists distribution as: Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

The FDA enforcement report describes the reason as: Undeclared allergen ingredient (Red#40)

Jovy Watermelon Gummy Rings was made or distributed by El Ruisenor De Mexico, INC. in Vernon, CA, United States. This page reflects FDA report H-0127-2027, dated October 28, 2026.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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 is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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 Jovy Watermelon Gummy Rings recall?

El Ruisenor De Mexico, INC. recalled Jovy Watermelon Gummy Rings in an FDA Class III enforcement action reported as H-0127-2027. Undeclared allergen ingredient (Red#40)

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.

Is the El Ruisenor De Mexico, INC. recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0127-2027. 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 El Ruisenor De Mexico, INC.

View brand

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