Med Man Distribution, Inc. recalls Bow & Arrow, Dietary Supplement, Libido Enhancer for Men, a) Four pack, b) Ten pack capsules per carton, Exclusively
Med Man's Bow & Arrow libido supplement contains undeclared sildenafil, a prescription drug. FDA found it without proper approval. Consumers should stop using and contact for details.
Recall notice
Marketed without an Approved NDA/ANDA: Product contains undeclared sildenafil which was discovered through FDA analysis.
Contact the company & request your remedy
What happened, in plain English
Med Man's Bow & Arrow dietary supplement for men contains undeclared sildenafil, a prescription drug that was found by the FDA without proper approval. This product is being recalled because it was marketed without an approved drug application, which could lead to health risks. Read more at govinfonow.com/recall/37746-med-man-bow-arrow-dietary-supplement-recall-undeclared-sildenafil-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37746-med-man-bow-arrow-dietary-supplement-recall-undeclared-sildenafil-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1037-2020
Cite this page
“Med Man Bow & Arrow Dietary Supplement Recall: Undeclared Sildenafil Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37746-med-man-bow-arrow-dietary-supplement-recall-undeclared-sildenafil-risk. Based on FDA recall #D-1037-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1037-2020%22&limit=1).
Why it’s dangerous
The supplement contains sildenafil, a prescription drug for erectile dysfunction, which was not approved by the FDA. This means it could cause serious health issues like heart problems or interactions with other medications without proper medical oversight.
Who’s affected
Men who purchased the Bow & Arrow dietary supplement in four-pack or ten-pack formats from Med Man Distribution. Those with underlying health conditions or who take other medications may be at higher risk.
How to tell if you have this one
Check for Bow & Arrow dietary supplements in four-pack or ten-pack formats sold exclusively by Med Man Distribution. All lots of this product are affected.
- Brand
Med Man- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Nationwide in the USA
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1036-2020 | 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.; All lots | 1,680 cartons |
| D-1037-2020 | Bow & Arrow, Dietary Supplement, Libido Enhancer for Men, a) Four pack, b) Ten pack capsules per carton, Exclusively Manufactured by: Medicine Man Distribution, 4234 I-75 Business Spur, Sault Ste Marie, MI 49783; All lots | 1880 cartons |
What to do — step by step
Stop Using Now
The product contains undeclared sildenafil, which was discovered by the FDA without proper approval. This could cause serious health risks.
Questions people ask
Is this product safe to use?
No, the FDA found undeclared sildenafil in this product, which is a prescription drug. It was not approved by the FDA and could cause serious health risks.
How can I check if I have the recalled product?
Check for Bow & Arrow dietary supplements in four-pack or ten-pack formats sold exclusively by Med Man Distribution. All lots are affected.
What should I do if I have this product?
Stop using it now and contact Med Man Distribution for further instructions.
Contact Med Man
We’ve drafted a message you can send Med Man to request your refund or repair — edit it as you like.
Subject: Recall D-1037-2020 — Med Man Med Man Hello, I own a Med Man that is covered by recall D-1037-2020 from Med Man. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1037-2020 (November 8, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1037-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.