FDA Drug recall D-1143-2017
ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg) capsule, packaged in 60-count bottle, Amazon.com, UPC 6 42125 50292…
- FDA Drug
- Class I
- terminated
- Published 2017-09-20
On 2017-09-20 the FDA classified a Class I recall of ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg) capsule, packaged in 60-count bottle, Amazon.com, UPC 6 42125 50292… by Andropharm, citing marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1143-2017 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2017-06-06 |
| Published | 2017-09-20 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Andropharm |
| Distribution | FL |
Product
ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg) capsule, packaged in 60-count bottle, Amazon.com, UPC 6 42125 50292 4
Reason
Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.
Identifiers
| upc | 642125502924 |
|---|---|
| code_info | All lots remaining within expiry. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1143-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.