# FDA recall D-1344-2019

> **SELECT DISTRIBUTIONS LLC** · Class I · drug recall initiated 2019-04-09.

## Product

Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by:  APhrodisiac. UPC Code 644118128135

## Reason for recall

Marketed without an approved NDA/ANDA: FDA analysis has found the product to be tainted with sildenafil

## Distribution

MI, OH

## Key facts

- **Recall number:** D-1344-2019
- **Recalling firm:** SELECT DISTRIBUTIONS LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-04-09
- **Report date:** 2019-06-19
- **Termination date:** 2023-10-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ferndale, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1344-2019

## Citation

> AI Analytics. FDA recall D-1344-2019. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/D-1344-2019. Source: US FDA. Licensed CC0.

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