Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Actra-SX 500 Capsules Recalled by Body Basics Inc Due to Marketed without an Approved NDA/ANDA; product contains sildenafil,...

Date: December 19, 2011
Company: Body Basics Inc
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Body Basics Inc directly.

Affected Products

Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA

Quantity: 30,000 capsules

Why Was This Recalled?

Marketed without an Approved NDA/ANDA; product contains sildenafil, an active ingredient in a FDA approved product for the treatment of Erectile Dysfunction

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Body Basics Inc

Body Basics Inc has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report