Bow and Arrow Libido Supplement Recalled for Undeclared Sildenafil
Med Man Distribution is recalling Bow & Arrow dietary supplements because they contain undeclared sildenafil, a prescription drug ingredient not listed on the label.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class I, which indicates a reasonable probability that the product will cause serious adverse health consequences or death. Additionally, the presence of undeclared sildenafil in a dietary supplement constitutes a significant injury risk.
Plain-English summary
The U.S. Food and Drug Administration (FDA) has announced a Class I recall of Bow & Arrow, a dietary supplement marketed as a libido enhancer for men. The product is exclusively manufactured by Med Man Distribution, Inc., located in Sault Ste Marie, Michigan.
The recall was initiated because FDA analysis discovered that the product contains undeclared sildenafil. Sildenafil is the active ingredient in prescription medications used to treat erectile dysfunction and pulmonary arterial hypertension. Its presence in an unapproved dietary supplement poses a risk of adverse health effects, particularly for individuals taking nitrates or those with heart conditions.
The affected products include both four-pack and ten-pack cartons of capsules. The recall covers all lots of the product distributed nationwide throughout the United States. A total of 1,880 cartons are involved in this recall.
Consumers who possess Bow & Arrow dietary supplements are advised to stop using the product immediately and return it to the place of purchase for a refund. Individuals with questions about the recall should contact Med Man Distribution, Inc. at the address listed on the packaging or via the FDA's drug recalls website.
The recalled product
- Product
- 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
- Manufacturer
- Med Man Distribution, Inc.
- Affected units
- 1,880
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All lots
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Med Man Distribution, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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