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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