# FDA recall D-1364-2014

> **Vitality Research Labs LLC** · Class I · drug recall initiated 2013-11-19.

## Product

vitaliKOR Ready When You Are, Fast Acting Formula Dietary Supplement capsules, 40 count bottle, Distributed by Vitality Research Labs, LLC, Las Vegas, NV 89148.

## Reason for recall

Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared  vardenafil and tadalafil in vitaliKOR capsules

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1364-2014
- **Recalling firm:** Vitality Research Labs LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-11-19
- **Report date:** 2014-06-18
- **Termination date:** 2014-06-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Las Vegas, NV, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1364-2014

## Citation

> AI Analytics. FDA recall D-1364-2014. Retrieved 2026-05-29 from https://api.ai-analytics.org/recall/D-1364-2014. Source: US FDA. Licensed CC0.

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