• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Enforcement Report - Week of September 11, 2013

  • Print
  • Share
  • E-mail

Product Detail

Product Description 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
Recall Number D-930-2013
Classification Class I
Code Info All lots of product distributed and sold from January 2012 to May 7, 2013. SKUs: SKUs 626570613855, 626570619055, 626570617860, 626570617563
Product Distributed Qty 145,632 capsules
Reason For Recall 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

Event Detail

Event Id 65130
Product Type Drugs
Status Ongoing
Recalling Firm Beamonstar Products
City Queen Creek
State AZ
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2013-05-01
Initial Firm Notification of Consignee or Public E-Mail
Distribution Pattern US states nationwide and international.