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

FDA recall notice · announced April 24, 2013 · Body Basics

Class I FDA/FSIS Class I: reasonable probability that use will cause serious adverse health consequences or death.

The product

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

Reason for recall

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

Notes

Distribution: Nationwide
Lot/code information: Lot number 008A, expiration date Dec 2014, UPC code 830733002016
Quantity: 30,000 capsules
Status: Terminated
Products in this recall event:
- Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA (D-265-2013)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.