Drug & medication recalls High risk

Bow & Arrow recalled over undeclared sildenafil

Recall date
November 8, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Med Man Distribution, Inc. recalls Bow & Arrow, Dietary Supplement, Libido Enhancer for Men, a) Four pack, b) Ten pack capsules per carton, Exclusively Ma…
Recall number
D-1037-2020
FDA classification
Class I
Brand / firm
Med Man Distribution, Inc.
Sold / distributed
Nationwide in the USA

Why it was recalled

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

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

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

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