Atlas Operations Recalls Sexual Enhancement Products

Atlas Operations, Inc., has announced it is recalling its dietary supplements for sexual enhancement sold under specific lot numbers.
These products are currently being sold as a dietary supplement throughout the US after FDA lab analyses found certain batches contain sulfoaildenafil, an analogue of sildenafil, an FDA-approved drug used as treatment for erectile dysfunction. The presence of this ingredient makes these products unapproved drugs.

Furthermore, the active drug ingredient is not listed on the product label. This undeclared ingredient may pose a threat to the consumer because the interaction of the analogue with some prescription drugs (such as nitroglycerin) may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol or heart disease often take other prescription drugs. Erectile dysfunction is a common problem in men with these conditions, and consumers may seek these types of products to enhance sexual performance.

These products are subject to the recall:

• Amour for him (lot number ###-705-##)
• APL (lot number ###-705-##)
• Arousin (lot number ###-705-##)
• Aspire One (lot number ###-494-##)
• Clyamax (lot number ###-705-##)
• Depth Charge (lot number ###-807-##)
• Enhancement (lot number ###-705-##)
• Erexa (lot number ###-705-##)
• Erexxx (lot number ###-705-##)
• Erousa (lot number ###-705-##)
• Ezerex (lot number ###-705-##)
• Finally On Demand (lot number ###-706-##)
• Libiplus (lot number ###-705-##)
• Love Fuel (lot numbers ###-520B-##, ###-520A-## and ###-706-##)
• Love Fuel 2 (lot number ###-521-##)
• Rainbow Rocket (lot number ###-706-##)
• Red Hot Sex (lot number ###-705-##)
• Rockhard (lot number ###-705-##)
• Sex Enhancer (lot number ###-520C-##)
• Sexual Surge (lot numbers ###-520B-##, ###-520A-## and ###-705-##)
• Staminil (lot numbers ###-520B-##, ###-520A-## and ###-705-##)
• Tacktol (lot number ###-705-##)
• Topviril (lot number ###-705-##)
• Vaxitrol (lot number ###-520-##)
• Vierect (lot number ###-705-##)
• Whatzup (lot number ###-706-##)
• Xtremexcite (lot number ###-706-##)
• Zenerect (lot number ###-705-##)
• 72 Hours (lot number ###-705-##)

The lot numbers may or may not contain dashes. The first three and last two digits and letters are insignificant.

If consumers have you a product with a different name but one of the lot numbers listed above, they should contact Atlas Operations for recall instructions.

Consumers who have purchased these products should discontinue their use and return the products to the place of purchase. Products can also be returned directly to Atlas Operations. Information about the recall are available by calling the company at 800-466-4444 Monday through Friday from 9 a.m. until 5 p.m. EST.

Adverse reaction or quality problems experienced with this product may be reported to the FDA's MedWatch Adverse Event Reporting program:

• Online:  www.fda.gov/MedWatch/report.htm
• Postal mail: Use postage-paid FDA form 3500 and mail to the address on the form
• Fax: 1-800-FDA-0178

Contact:
Daniel Kinney
954-788-1200