UP2 — Class I drug recall D-1036-2020
Terminated recall by Med Man Distribution, Inc., reported 2020-03-25, distributed nationwide. Marketed without an Approved NDA/ANDA: Product contains undeclared sildenafil which was discovered through FDA
| Recall number | D-1036-2020 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Med Man Distribution, Inc., Pickerel, Canada |
| Recall initiated | 2019-11-08 |
| Classified | 2020-03-19 |
| Reported by FDA | 2020-03-25 |
| Terminated | 2023-10-17 |
| Distributed | Nationwide (US) |
| Quantity | 1,680 cartons |
| Reason classes | undeclared allergen, unapproved product |
| Lot numbers | UP2 |
Product
UP2, Dietary Supplement, All Natural Libido for Men & Women, a) one pack, b) four pack, c) ten pack capsules per carton, Exclusively Manufactured and Formulated by: Buy Wise Marketing, 4234 I-75 Business Spur, Sault Ste Marie, MI 49783, Ultimatepleasure2.com.
Reason for recall
Marketed without an Approved NDA/ANDA: Product contains undeclared sildenafil which was discovered through FDA analysis.
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-1036-2020. 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.