Enhanced Vegetal Vigra 200 mg Capsules — Class I drug recall D-0149-2018
Terminated recall by Natures Supplement, reported 2018-01-10, distributed in FL. Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with Sildenafil.
| Recall number | D-0149-2018 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Natures Supplement, Lake Worth, FL, United States |
| Recall initiated | 2017-09-20 |
| Classified | 2018-01-04 |
| Reported by FDA | 2018-01-10 |
| Terminated | 2019-05-01 |
| Distributed | FL |
| Quantity | 308 bottles |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 08931028556885 |
| Expiration dates | 2020-02-23 |
Product
Enhanced Vegetal Vigra 200 mg Capsules, 8 count bottles, Manufacturer: Hand-shaking (Int'l) Cop. USA, ADD: Hand-shaking Mansion, the 5th Ave., Stanford, USA --- UPC# 8931028556885
Reason for recall
Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with 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-0149-2018. 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.