Evil Root 1200 mg — Class I drug recall D-376-2014
Terminated recall by Fabscout Entertainment, Inc, reported 2013-12-25, distributed in CA, FL, UT. Marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil
| Recall number | D-376-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fabscout Entertainment, Inc, Ft Lauderdale, FL, United States |
| Recall initiated | 2013-08-14 |
| Classified | 2013-12-18 |
| Reported by FDA | 2013-12-25 |
| Terminated | 2021-02-10 |
| Distributed | CA, FL, UT |
| Reason classes | undeclared allergen, unapproved product |
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 for recall
Marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-376-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.