FDA Drug recall D-376-2014
Evil Root 1200 mg, supplied in 6 capsules per bottle, Manufacturer: Tibet Shengyang Health Medicine Co.,Ltd
- FDA Drug
- Class I
- terminated
- Published 2013-12-25
On 2013-12-25 the FDA classified a Class I recall of Evil Root 1200 mg, supplied in 6 capsules per bottle, Manufacturer: Tibet Shengyang Health Medicine Co.,Ltd by Fabscout Entertainment, citing marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-376-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-08-14 |
| Published | 2013-12-25 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Fabscout Entertainment |
| Distribution | CA, FL, UT |
Product
Evil Root 1200 mg, supplied in 6 capsules per bottle, Manufacturer: Tibet Shengyang Health Medicine Co.,Ltd. Address: No. 98, Min zu Road, Lhasa
Reason
Marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil
Identifiers
| code_info | All Lots |
|---|
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-376-2014%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.