Boner Bears · Chocolate

No lo uses. Devuélvelo a la tienda o bótalo. Si te sentiste mal después de usarlo, llama a tu médico y dile qué tomaste.

Lotes o códigos

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…

Lot Number: BB21125

Expiration Date: 02/2026

Copiado tal como lo dice el aviso oficial, en su idioma.

Compara la marca, el tamaño, la fecha y el número de lote de tu producto con el aviso oficial.

JXK Enterprises, Inc retiró este producto. Motivo: Contiene un medicamento no aprobado.

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.

Tiene un medicamento que no aparece en la etiqueta. Puede ser peligroso, sobre todo si tomas otras medicinas.

En todo EE. UU. (distribución nacional). El aviso no nombra Puerto Rico, pero pudo haber llegado aquí.

Según el aviso: Boner Bears Chocolate is marketed as a sexual enhancement product and was distributed nationwide via online sales.

FDA recall announcement: JXK Enterprises, Inc Issues Voluntary Nationwide Recall of Boner Bears Chocolate Due to Undeclared Sildenafil Company: JXK Enterprises, Inc Product: Chocolate (brand: Boner Bears) Reason: Product contains sildenafil [Unapproved Ingredient] Distribution: Boner Bears Chocolate is marketed as a sexual enhancement product and was distributed nationwide via online sales. Codes: 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 F