# FDA recall D-323-2013

> **D& S Herbals, LLC** · Class I · drug recall initiated 2012-12-22.

## Product

Super Power capsules, Proprietary Blend 570 mg, packaged in 2-count capsules per blister pack, Distributed by: Freedom Trading, NJ 08863, UPC 7 18122 90678 9.

## Reason for recall

Marketed Without An Approved NDA/ANDA: This dietary supplement has been found to contain sildenafil, an FDA approved drug for the treatment of male erectile dysfunction making this an unapproved new drug.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-323-2013
- **Recalling firm:** D& S Herbals, LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-12-22
- **Report date:** 2013-05-22
- **Termination date:** 2013-08-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Woodbridge, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-323-2013

## Citation

> AI Analytics. FDA recall D-323-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-323-2013. Source: US FDA. Licensed CC0.

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