SexVoltz All Natural Herbal Supplement — Class I drug recall D-929-2013
Terminated recall by Beamonstar Products, reported 2013-09-11, distributed nationwide. Marketed Without an Approved NDA/ANDA; products have been found to contain tadalafil, the active ingredient in
| Recall number | D-929-2013 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beamonstar Products, Queen Creek, AZ, United States |
| Recall initiated | 2013-05-01 |
| Classified | 2013-09-05 |
| Reported by FDA | 2013-09-11 |
| Terminated | 2014-04-21 |
| Distributed | Nationwide (US) |
| Quantity | 673,851 capsules |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 00626570609490, 00626570615316, 00626570617877, 00626570623588, 00827912089028 |
Product
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
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-929-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.