FDA Drug recall D-1236-2014
PHUK Sexual Enhancement Ultimate Pleasure, 400mg/capsule, packaged in 1 and 2 capsule blister packs and 4,12,24 capsule bottles, Distribute…
- FDA Drug
- Class I
- terminated
- Published 2014-04-23
On 2014-04-23 the FDA classified a Class I recall of PHUK Sexual Enhancement Ultimate Pleasure, 400mg/capsule, packaged in 1 and 2 capsule blister packs and 4,12,24 capsule bottles, Distribute… by Haute Health, citing marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of active ingredients found in some FDA-approved drugs for erectile dysfunction (ED) making the dieta….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1236-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-09-27 |
| Published | 2014-04-23 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Haute Health |
| Distribution | US |
Product
PHUK Sexual Enhancement Ultimate Pleasure, 400mg/capsule, packaged in 1 and 2 capsule blister packs and 4,12,24 capsule bottles, Distributed by UME Supplements, INC www.phukherbal.com.
Reason
Marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of active ingredients found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.
Identifiers
| code_info | All lot codes and expiration dates. |
|---|
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-1236-2014%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.