JXK Enterprises, Inc Issues Voluntary Nationwide Recall of Boner Bears Chocolate Due to Undeclared Sildenafil

COMPANY ANNOUNCEMENT JXK Enterprises, Inc Issues Voluntary Nationwide Recall of Boner Bears Chocolate Due to Undeclared Sildenafil When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Read Announcement View Product PhotosSummary - Company Announcement Date: - FDA Publish Date: - Product Type: - Food & Beverages Ingredients - Reason for Announcement: - Recall Reason DescriptionProduct contains sildenafil - Company Name: - JXK Enterprises, Inc - Brand Name: - Brand Name(s)Boner Bears - Product Description: - Product DescriptionChocolate Company Announcement 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. Sildenafil is approved for use only under the supervision of a licensed healthcare professional for the treatment of erectile dysfunction. Products containing undeclared sildenafil may pose serious health risks. Sildenafil can interact with nitrates found in certain prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. Individuals with diabetes, high blood pressure, high cholesterol, or heart disease are at increased risk due to potential interactions. Boner Bears Chocolate is marketed as a sexual enhancement product and was distributed nationwide via online sales. (https://www.elyxr.com/) The recalled product can be identified as: - 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.” No other lots or products are included in this recall. JXK Enterprises, Inc has not received any reports of adverse events related to this recall to date. Consumers who have purchased the recalled product are urged to stop using it immediately and contact the company for instructions on return and refund. Consumers with questions may contact: JXK Enterprises, Inc Phone: (954) 281-2459 Email: compliance@elyxr.com Hours: [Mon–Fri, 9 AM–6 PM PST] 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: www.fda.gov/medwatch/report.htm Phone: 1-800-332-1088 This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.