Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

© 2026 Go Backs. All rights reserved.

Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Med Man Distribution, Inc.: UP2 and Bow & Arrow Supplements Recalled for Undeclared Sildenafil

Agency Publication Date: March 19, 2020
Share:
Sign in to monitor this recall

Summary

Med Man Distribution, Inc. is recalling approximately 3,560 units of UP2 and Bow & Arrow dietary supplements because they contain sildenafil, an undeclared ingredient that is the active component in the prescription drug Viagra. These products were marketed as natural libido enhancers for men and women but were found to contain the hidden drug during FDA laboratory analysis. Consumers should immediately stop using these products, which were sold nationwide in various pack sizes ranging from single capsules to ten-pack cartons.

Risk

The undeclared sildenafil poses a serious health risk because it may interact with nitrates found in some prescription drugs (such as nitroglycerin) and can lower blood pressure to dangerous or life-threatening levels. This is particularly dangerous for individuals with diabetes, high blood pressure, high cholesterol, or heart disease who often take nitrates.

What You Should Do

  1. Check your supplement supply for UP2 (All Natural Libido for Men & Women) and Bow & Arrow (Libido Enhancer for Men) capsules.
  2. For UP2, identify affected products by checking for 1-pack, 4-pack, or 10-pack cartons labeled 'Exclusively Manufactured and Formulated by: Buy Wise Marketing' with website Ultimatepleasure2.com.
  3. For Bow & Arrow, identify affected products by checking for 4-pack or 10-pack cartons labeled 'Exclusively Manufactured by: Medicine Man Distribution' with address 4234 I-75 Business Spur, Sault Ste Marie, MI.
  4. Note that this recall applies to all lot numbers for both UP2 (Recall #: D-1036-2020) and Bow & Arrow (Recall #: D-1037-2020).
  5. Stop using these products immediately and return any unused portions to the place of purchase for a refund.
  6. Contact your healthcare provider or pharmacist for guidance if you have consumed these products and have concerns about your health.
  7. Contact Med Man Distribution, Inc. for further instructions regarding the return process or refund details.
  8. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Full refund for unused product

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: UP2 Dietary Supplement, All Natural Libido for Men & Women (1 pack)
Model:
D-1036-2020
Lot Numbers:
All lots
Product: UP2 Dietary Supplement, All Natural Libido for Men & Women (4 pack)
Model:
D-1036-2020
Lot Numbers:
All lots
Product: UP2 Dietary Supplement, All Natural Libido for Men & Women (10 pack)
Model:
D-1036-2020
Lot Numbers:
All lots
Product: Bow & Arrow Dietary Supplement, Libido Enhancer for Men (4 pack)
Model:
D-1037-2020
Lot Numbers:
All lots
Product: Bow & Arrow Dietary Supplement, Libido Enhancer for Men (10 pack)
Model:
D-1037-2020
Lot Numbers:
All lots

Product Images

Label, Up2 there is no other All Natural Libido for Men & Women, Ten Pack

Label, Up2 there is no other All Natural Libido for Men & Women, Ten Pack

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84265
Status: Resolved
Manufacturer: Med Man Distribution, Inc.
Sold By: Ultimatepleasure2.com
Manufactured In: Canada
Units Affected: 2 products (1,680 cartons; 1880 cartons)
Distributed To: Nationwide
Agency Last Updated: October 17, 2023

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.