FDA Drug recall D-1335-2014
BOOST ULTRA, sexual enhancement dietary supplement, 12-capsule/bottle
- FDA Drug
- Class I
- terminated
- Published 2014-05-28
On 2014-05-28 the FDA classified a Class I recall of BOOST ULTRA, sexual enhancement dietary supplement, 12-capsule/bottle by Schindele Enterprises, citing marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1335-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-01-09 |
| Published | 2014-05-28 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Schindele Enterprises |
| Distribution | CA, CT, FL, GA, IA, IL, LA, MD, NV, NY, PA, TX, WI |
Product
BOOST ULTRA, sexual enhancement dietary supplement, 12-capsule/bottle. Also packaged in 3 pill bottles and 1 pill packs. BoostUtra.com, Springfield, MO.
Reason
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Identifiers
| code_info | 12 pill bottle and 3 pill bottle: Lot # B70130 Exp. 03/15; 1 pill pack: Lot # 06012011 Exp 06/14. |
|---|
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-1335-2014%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.