# FDA recall D-265-2013

> **Body Basics Inc** · Class I · drug recall initiated 2011-12-19.

## Product

Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA

## Reason for recall

Marketed without an Approved NDA/ANDA; product contains sildenafil, an active ingredient in a FDA approved product for the treatment of Erectile Dysfunction

## Distribution

Nationwide

## Key facts

- **Recall number:** D-265-2013
- **Recalling firm:** Body Basics Inc
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2011-12-19
- **Report date:** 2013-04-24
- **Termination date:** 2013-06-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Canoga Park, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-265-2013

## Citation

> AI Analytics. FDA recall D-265-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-265-2013. Source: US FDA. Licensed CC0.

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