# FDA recall D-345-2014

> **Myson Corporation, Inc.** · Class I · drug recall initiated 2013-07-19.

## Product

Volcano Male Enhancement 1500mg, 1-count capsule packaged in a black round plastic pop top container, (Proprietary Formula, Pueraria lobata, Cinnamon Bark, Cuscuta, Gui, Licorice, Altractylodes, Dang Condonopsis, Dismutase, Cornus, Rubus, Deng Sen Extract, Panax Ginseng, Cordyceps Sinensis, Go Ji Extract, Superoxide Dismutase).

## Reason for recall

Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and Volcano Capsules, marketed as dietary supplements, are being recalled because they were found to contain undeclared active pharmaceutical ingredients, making them unapproved new drugs.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-345-2014
- **Recalling firm:** Myson Corporation, Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-07-19
- **Report date:** 2013-12-18
- **Termination date:** 2015-01-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Long Beach, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-345-2014

## Citation

> AI Analytics. FDA recall D-345-2014. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-345-2014. Source: US FDA. Licensed CC0.

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