Plant Vigra — Class I drug recall D-0899-2016
Terminated recall by R Thomas Marketing, LLC, reported 2016-06-01, distributed nationwide. Marketed Without An Approved NDA/ANDA
| Recall number | D-0899-2016 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | R Thomas Marketing, LLC, Bronx, NY, United States |
| Recall initiated | 2016-01-09 |
| Classified | 2016-05-26 |
| Reported by FDA | 2016-06-01 |
| Terminated | 2019-06-21 |
| Distributed | Nationwide (US) |
| Reason classes | unapproved product |
Product
Plant Vigra, packaged in BIG BOX / (18 cans / 6 capsules per can / 108 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Reason for recall
Marketed Without An Approved NDA/ANDA
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-0899-2016. 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.