ACTIVE RECALL — CLASS IActive recallH-0186-2027/FDA enforcement

Boner Bears Chocolate, 3 Doses Per Bar, NET WT

What you need to know

Class I
  • What happened

    JXK Enterprises, Inc is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of sildenafil, an…

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A prescription drug ingredient hidden in a product sold as a supplement or food, creating serious cardiac risks.

  • 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.

Active recall · classified by the FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameJxk Enterprises, INC.
Recalling firmJxk Enterprises, INC.Miami, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot #BB21125
Distribution area
Nationwide

Boner Bears Chocolate is marketed as a sexual enhancement product and was distributed nationwide via online sales through www.elyxr.com.

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: November 4, 2026
FDA recall numberH-0186-2027

Beyond the headline

The recall, in context

Jxk Enterprises, INC. initiated this food recall on May 21, 2026. The FDA enforcement report states: JXK Enterprises, Inc is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of sildenafil, an active ingredient in the FDA-approved prescription drug Viagra, which is not declared on the product label. The FDA report lists distribution as: Boner Bears Chocolate is marketed as a sexual enhancement product and was distributed nationwide via online sales through www.elyxr.com.

The FDA enforcement report describes the reason as: JXK Enterprises, Inc is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of sildenafil, an active ingredient in the FDA-approved prescription drug Viagra, which is not declared on the product label.

Boner Bears Chocolate, 3 Doses Per Bar, NET WT was made or distributed by Jxk Enterprises, INC. in Miami, FL, United States. This page reflects FDA report H-0186-2027, dated November 4, 2026.

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 prescription drug ingredient hidden in a product sold as a supplement or food, creating serious cardiac risks.

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 lot and date codes 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 Boner Bears Chocolate, 3 Doses Per Bar, NET WT recall?

Jxk Enterprises, INC. recalled Boner Bears Chocolate, 3 Doses Per Bar, NET WT in an FDA Class I enforcement action reported as H-0186-2027. JXK Enterprises, Inc is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of sildenafil, an…

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?

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.

How do I get a refund from Jxk Enterprises, 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 H-0186-2027 and keep the packaging, lot code and proof of purchase if you have them.

Is the Jxk Enterprises, 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-0186-2027. 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

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