FDAFDA · Food and drugs·Recall number D-265-2013
Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA
Published April 24, 2013 · Recall initiated: December 19, 2011
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Marketed without an Approved NDA/ANDA; product contains sildenafil, an active ingredient in a FDA approved product for the treatment of Erectile Dysfunction
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Body Basics Inc
- Distributor
- Nationwide
- Lot
- Lot number 008A, expiration date Dec 2014, UPC code 830733002016
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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