# FDA recall D-333-2013

> **Performance Plus Marketing, Inc.** · Class I · drug recall initiated 2012-12-17.

## Product

libigrow XXXTREME Capsules, MAXIMUM STRENGTH FORMULA, 1000 mg, supplied in 1, 5 and 10 count blister packs, Distributed By Kretek International, Inc. Moorpark, CA 930210    1 count blister: UPC 705105830735,  5 count blister: UPC 610585435939,  10 count blister:  UPC 610585435922.

## Reason for recall

Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs

## Distribution

Nationwide

## Key facts

- **Recall number:** D-333-2013
- **Recalling firm:** Performance Plus Marketing, Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-12-17
- **Report date:** 2013-05-22
- **Termination date:** 2013-11-14

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-333-2013

## Citation

> AI Analytics. FDA recall D-333-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-333-2013. Source: US FDA. Licensed CC0.

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