# FDA recall D-1143-2017

> **Andropharm, LLC** · Class I · drug recall initiated 2017-06-06.

## Product

ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg) capsule, packaged in 60-count bottle, Amazon.com,  UPC 6 42125 50292 4

## Reason for recall

Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.

## Distribution

Florida

## Key facts

- **Recall number:** D-1143-2017
- **Recalling firm:** Andropharm, LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-06-06
- **Report date:** 2017-09-20
- **Termination date:** 2020-06-02

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1143-2017

## Citation

> AI Analytics. FDA recall D-1143-2017. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/D-1143-2017. Source: US FDA. Licensed CC0.

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