FDA Drug Critical Class I Terminated

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

Reported: September 20, 2017 Initiated: June 6, 2017 #D-1143-2017

Product Description

Reason for Recall

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

Details

Recalling Firm: Andropharm, LLC
Units Affected: 1250 bottles
Distribution: Florida
Location: Boca Raton, FL

Frequently Asked Questions

What product was recalled? ▼

ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg) capsule, packaged in 60-count bottle, Amazon.com, UPC 6 42125 50292 4. Recalled by Andropharm, LLC. Units affected: 1250 bottles.

Why was this product recalled? ▼

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

Which agency issued this recall? ▼

This recall was issued by the FDA Drug on September 20, 2017. Severity: Critical. Recall number: D-1143-2017.

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