CLASS I Drug recall · Reported 11 Sep 2013 · FDA Enforcement Report
SexVoltz All Natural Herbal Supplement recalled by Beamonstar Products
Beamonstar Products is recalling SexVoltz All Natural Herbal Supplement, distributed nationwide in the US. The recall was initiated on 1 May 2013 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-929-2013
- FDA event ID
- 65130
- Recalling firm
- Beamonstar Products, Queen Creek, AZ
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 1 May 2013
- FDA classified
- 5 Sep 2013
- Reported
- 11 Sep 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Hidden Drug Ingredients
Timeline
| 1 May 2013 | Recall initiated by company | |
| 5 Sep 2013 | Classified by FDA | +127 days |
| 11 Sep 2013 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
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
Where it was distributed
US states nationwide and international.
Questions about this recall
Why was it 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
Which lots are affected?
All lots of product distributed and sold from January 2012 to May 7, 2013 SKUs: 626570609490, 827912089028, 626570617877, 626570615316, 626570623588
Where was it sold?
US states nationwide and international.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 65130This product is part of a recall event; the main page for the event is Velextra All-Natural Herbal Supplement recalled by Beamonstar Products.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Velextra All-Natural Herbal Supplement recalled by Beamonstar Products | Beamonstar Products | Hidden Drug Ingredients | Nationwide |
More recalls from Beamonstar Products
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Velextra All-Natural Herbal Supplement recalled by Beamonstar Products | Beamonstar Products | Hidden Drug Ingredients | Nationwide |