FDA Drug recall D-930-2013
Velextra All-Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 & 12 capsule bottles, Manufactured For: BeaMonsta…
- FDA Drug
- Class I
- terminated
- Published 2013-09-11
On 2013-09-11 the FDA classified a Class I recall of Velextra All-Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 & 12 capsule bottles, Manufactured For: BeaMonsta… by Beamonstar Products, citing 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 t….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-930-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-05-01 |
| Published | 2013-09-11 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Beamonstar Products |
| Distribution | US |
Product
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
Reason
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
Identifiers
| code_info | All lots of product distributed and sold from January 2012 to May 7, 2013. SKUs: SKUs 626570613855, 626570619055, 626570617860, 626570617563 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-930-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.