FDAFDA · Food and drugs·Recall number D-930-2013
Velextra All-Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 & 12 capsule bottles, Manufactured For: BeaMonstar Products Queen Creek, AZ
Published September 11, 2013 · Recall initiated: May 1, 2013
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; products have been found to contain tadalafil, the active ingredient in an FDA approved product used to treat erectile dysfunction, making this product an unapproved drug
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Beamonstar Products
- Distributor
- US states nationwide and international.
- Lot
- All lots of product distributed and sold from January 2012 to May 7, 2013. SKUs: SKUs 626570613855, 626570619055, 626570617860, 626570617563
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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