# FDA recall D-344-2014

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

## Product

Volcano Male Enhancement Liquid, 2 FL OZ (60 ml) bottle, www.volcanoenhancement.com, DISTRIBUTED BY VOLCANO Long Beach, CA 90813, UPC 6 09613 85996 0.

## 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-344-2014
- **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-344-2014

## Citation

> AI Analytics. FDA recall D-344-2014. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-344-2014. Source: US FDA. Licensed CC0.

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