FUEL UP PLUS — Class I drug recall D-0959-2016
Terminated recall by Reesna, Inc, reported 2016-06-15, distributed nationwide. Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: Products were found t
| Recall number | D-0959-2016 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Reesna, Inc, Canoga Park, CA, United States |
| Recall initiated | 2015-12-11 |
| Classified | 2016-06-06 |
| Reported by FDA | 2016-06-15 |
| Terminated | 2016-06-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | GB |
| Quantity | 26,250 capsules |
| Reason classes | undeclared allergen, unapproved product |
Product
FUEL UP PLUS, capsules, a) 1-count package, b) 5-count bottle, c) 10-count bottle WWW.FUELUPPILLS.COM
Reason for recall
Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: Products were found to be tainted with undeclared hydroxythiohomosildenafil, an analogue of Sildenafil, an FDA-approved drug for the treatment of male Erectile Dysfunction (ED), making them unapproved new drugs.
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-0959-2016. 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.