CLASS I Drug recall · Reported 25 Mar 2020 · FDA Enforcement Report
UP2, Dietary Supplement, All Natural Libido for Men & Women recalled
Med Man Distribution is recalling UP2, Dietary Supplement, All Natural Libido for Men & Women, a) one pack, b) four pack, distributed nationwide in the US. The recall was initiated on 8 Nov 2019 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1036-2020
- FDA event ID
- 84265
- Recalling firm
- Med Man Distribution, Pickerel
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 8 Nov 2019
- FDA classified
- 19 Mar 2020
- Reported
- 25 Mar 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
Timeline
| 8 Nov 2019 | Recall initiated by company | |
| 19 Mar 2020 | Classified by FDA | +132 days |
| 25 Mar 2020 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an Approved NDA/ANDA: Product contains undeclared sildenafil which was discovered through FDA analysis.
Product as listed by the FDA
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.
Where it was distributed
Nationwide in the USA
Questions about this recall
Why was it recalled?
Marketed without an Approved NDA/ANDA: Product contains undeclared sildenafil which was discovered through FDA analysis.
Which lots are affected?
All lots
Where was it sold?
Nationwide in the USA
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 84265This product is part of a recall event; the main page for the event is Bow & Arrow, Dietary Supplement, Libido Enhancer for Men recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Bow & Arrow, Dietary Supplement, Libido Enhancer for Men recalled | Med Man Distribution | Labeling Errors | Nationwide |
More recalls from Med Man Distribution
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Bow & Arrow, Dietary Supplement, Libido Enhancer for Men recalled | Med Man Distribution | Labeling Errors | Nationwide |