FDA Drug recall D-1223-2014
Vicerex A Powerful And Fast Acting Male Sexual Enhancer, 10 capsules per box, Dietary Supplement
- FDA Drug
- Class I
- terminated
- Published 2014-04-16
On 2014-04-16 the FDA classified a Class I recall of Vicerex A Powerful And Fast Acting Male Sexual Enhancer, 10 capsules per box, Dietary Supplement by American Lifestyle Com, citing marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1223-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-04-30 |
| Published | 2014-04-16 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | American Lifestyle Com |
| Distribution | n/a |
Product
Vicerex A Powerful And Fast Acting Male Sexual Enhancer, 10 capsules per box, Dietary Supplement. UPC 893490820087 (product numbers may possibly vary for same product identification and same product packaging), distributed by Vicerex.com.
Reason
Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains undeclared sildenafil. Tadalafil and sildenafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the Vicerex and the Black Ant products unapproved new drugs.
Identifiers
| upc | 893490820087 |
|---|---|
| code_info | All lots, UPC 893490820087 |
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-1223-2014%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.