# FDA recall D-021-2014

> **Jack Rabbit, Inc** · Class I · drug recall initiated 2013-08-12.

## Product

J.R.  Jack Rabbit All Natural Herbal Supplement, One tablet can last 24-72 hours, 4-count tablets per blister pack, Order at: www.jackrabbitfourpack.com, Jack Rabbit Inc., 4355 Dow Road, Melbourne, FL 32934

## Reason for recall

Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined that J.R.  Jack Rabbit Male Enhancement product was found to contain two undeclared  active pharmaceutical ingredients: sildenafil and tadalafil.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-021-2014
- **Recalling firm:** Jack Rabbit, Inc
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-08-12
- **Report date:** 2013-12-04
- **Termination date:** 2020-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Melbourne, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-021-2014

## Citation

> AI Analytics. FDA recall D-021-2014. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-021-2014. Source: US FDA. Licensed CC0.

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