Class I — Most Severe

Boner Bears Chocolate Recalled for Undeclared Sildenafil

FreshRecall Team JXK Enterprises, Inc Undeclared Drug
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Class I Recall — Most Serious

This is a Class I recall — the most serious type. Products covered by this recall may cause serious health consequences or death.

Image of front label, Boner Bears Sex Chocolate, Net Wt 22g Image of back label, Boner Bears Sex Chocolate Lot Number: BB21125

JXK Enterprises, Inc has issued a voluntary nationwide recall of its Boner Bears Chocolate due to the presence of undeclared sildenafil. This ingredient, found in the prescription drug Viagra, is not listed on the product label and can pose serious health risks.

Affected Product Details:

  • Product Name: Boner Bears Sex Chocolate
  • Lot Number: BB21125
  • Expiration Date: 02/2026
  • Net Weight: 22g
  • Packaging: Individually wrapped chocolate bar in a black wrapper labeled “Boner Bears Sex Chocolate,” “Fast Acting Max Strength,” and “3 Doses Per Bar.”

The recall affects products distributed nationwide through online sales. No other lots or products are included in this recall.

Reason for Recall:

The recall was initiated after FDA laboratory analysis confirmed the presence of sildenafil, which is approved for use only under the supervision of a licensed healthcare professional for the treatment of erectile dysfunction. Sildenafil can interact with nitrates found in certain prescription drugs, such as nitroglycerin, potentially lowering blood pressure to dangerous levels. Individuals with diabetes, high blood pressure, high cholesterol, or heart disease are at increased risk.

Consumer Guidance:

Consumers who have purchased the recalled product should stop using it immediately and contact JXK Enterprises, Inc for instructions on return and refund. The company can be reached at (954) 281-2459 or via email at [email protected], Monday through Friday, 9 AM–6 PM PST.

No adverse events related to this recall have been reported to date. However, any adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program online or by phone at 1-800-332-1088.

This recall is conducted with the knowledge of the U.S. Food and Drug Administration.

Where Products Were Sold

This recall affects products distributed nationwide across the United States.

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View original FDA announcement