# FDA recall D-929-2013

> **Beamonstar Products** · Class I · drug recall initiated 2013-05-01.

## Product

SexVoltz All Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 and 12 capsule bottles, Manufactured For: BeaMonstar Products, Queen Creek, AZ

## Reason for recall

Marketed Without an Approved NDA/ANDA; products have been found to contain tadalafil, the active ingredient in an FDA approved product used to treat erectile dysfunction, making this product an unapproved drug

## Distribution

US states nationwide and international.

## Key facts

- **Recall number:** D-929-2013
- **Recalling firm:** Beamonstar Products
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-05-01
- **Report date:** 2013-09-11
- **Termination date:** 2014-04-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Queen Creek, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-929-2013

## Citation

> AI Analytics. FDA recall D-929-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-929-2013. Source: US FDA. Licensed CC0.

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