Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Terminated Initiated Nov 8, 2019 (7 years ago)

Bow & Arrow

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Marketed without an Approved NDA/ANDA: Product contains undeclared sildenafil which was discovered through FDA analysis.

Cause type: Chemical / undeclared

A chemical that should not be there - benzene, methanol, lead - or an undeclared prescription drug hidden in a supplement. The label gives no warning: you may be taking a toxic solvent, a heavy metal, or a drug such as sildenafil that interacts with your other medicines. All chemical / undeclared recalls.

What was recalled

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

Recalling firm
Med Man Distribution, Inc.
Origin
Canada
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1037-2020 · FDA notice

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Med Man Distribution, Inc.

All 2019 recalls
Class I · High risk

UP2, Dietary Supplement

Marketed without an Approved NDA/ANDA: Product contains undeclared sildenafil which was discovered through FDA analysis.

Terminated Chemical / undeclared Med Man Distribution, Inc. D-1036-2020

Other chemical / undeclared recalls from 2019

All chemical / undeclared recalls