Aphrodisiac Platinum 40000 — Class I drug recall D-1344-2019
Terminated recall by SELECT DISTRIBUTIONS LLC, reported 2019-06-19, distributed in MI, OH. Marketed without an approved NDA/ANDA: FDA analysis has found the product to be tainted with sildenafil
| Recall number | D-1344-2019 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SELECT DISTRIBUTIONS LLC, Ferndale, MI, United States |
| Recall initiated | 2019-04-09 |
| Classified | 2019-06-13 |
| Reported by FDA | 2019-06-19 |
| Terminated | 2023-10-16 |
| Distributed | MI, OH |
| Quantity | 60 boxes |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 00644118128135 |
Product
Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by: APhrodisiac. UPC Code 644118128135
Reason for recall
Marketed without an approved NDA/ANDA: FDA analysis has found the 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-1344-2019. 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.