US Drug Recall Register
Class I · High risk Terminated Initiated May 1, 2013 (13 years ago)

SexVoltz All Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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 was recalled

SexVoltz All Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 and 12 capsule bottles, Manufactured For: BeaMonstar Products, Queen Creek, AZ

Recalling firm
Beamonstar Products
Origin
AZ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-929-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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