# FDA recall D-1321-2019

> **Stiff Boy LLC** · Class I · drug recall initiated 2019-05-06.

## Product

The Beast, The Beast can be taken under the situation of Heart disease and even after drinking, 4600 mg X 4 Capsules per packet.

## Reason for recall

Marketed without an Approved NDA/ANDA: The Beast contains undeclared sildenafil which was discovered through FDA analysis.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1321-2019
- **Recalling firm:** Stiff Boy LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-05-06
- **Report date:** 2019-06-05
- **Termination date:** 2025-09-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Englewood, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1321-2019

## Citation

> AI Analytics. FDA recall D-1321-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-1321-2019. Source: US FDA. Licensed CC0.

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