# FDA recall D-165-2013

> **P & J Trading Co** · Class I · drug recall initiated 2012-12-19.

## Product

SLIMDIA Revolution capsules, 30-count capsules per bottle, Yerba Naturals, 19685 Varda Ave., Buena Park, CA.

## Reason for recall

Marketed Without an Approved NDA/ANDA: All lots of the dietary supplement Slimdia Revolution are being recalled because they contain sibutramine, a previously approved FDA drug removed from the U.S. marketplace for safety reasons, making it an unapproved new drug.

## Distribution

Korea

## Key facts

- **Recall number:** D-165-2013
- **Recalling firm:** P & J Trading Co
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-12-19
- **Report date:** 2013-02-27
- **Termination date:** 2013-03-25

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-165-2013

## Citation

> AI Analytics. FDA recall D-165-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-165-2013. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
