Andropharm M1 Alpha Capsules: Unapproved Steroid Product Recalled
Andropharm recalls 60-count M1 Alpha capsules marketed without FDA approval as containing anabolic steroids. Consumers should check product labels and contact the company for details.
Recall notice
Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.
Contact the company
What happened, in plain English
Andropharm is recalling 60-count bottles of M1 Alpha capsules because they were sold without FDA approval and labeled as containing anabolic steroids. This could lead to health risks if used without proper medical supervision. Read more at govinfonow.com/recall/41580-andropharm-m1-alpha-capsules-unapproved-steroid-product-recalled.
Source Summary by GovInfoNow · govinfonow.com/recall/41580-andropharm-m1-alpha-capsules-unapproved-steroid-product-recalled · Updated October 8, 2026 · FDA enforcement record: FDA #D-1143-2017
Cite this page
“Andropharm M1 Alpha Capsules: Unapproved Steroid Product Recalled.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41580-andropharm-m1-alpha-capsules-unapproved-steroid-product-recalled. Based on FDA recall #D-1143-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1143-2017%22&limit=1).
Why it’s dangerous
The product was marketed without FDA approval and labeled as containing anabolic steroids. Anabolic steroids can cause serious health issues like liver damage, heart problems, and hormonal imbalances if misused.
Who’s affected
Anyone who purchased the 60-count bottle of Andropharm M1 Alpha capsules from Amazon. People using these capsules for medical purposes without a prescription are at higher risk.
How to tell if you have this one
Check for the 60-count bottle labeled 'ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg)'. The product was sold on Amazon with UPC 642125502924.
- Brand
Andropharm- Product
ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg) capsule, packaged in 60-count bottle- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Florida
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1142-2017 | ANDROPHARM STEN Z (2, 17a-Dimethyl-17b-hydroxy-5a-androst-1-en-3-one 10mg and 17b-hydroxy-2a, 17b-dimethyl-5a-androstan-3-one azine 10 mg) capsule, packaged in 60-count bottle, Andropharm.com, UPC: 6 42125 50294 8; All lots remaining within expiry. | 150 bottles |
| D-1143-2017 | ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg) capsule, packaged in 60-count bottle, Amazon.com, UPC 6 42125 50292 4; All lots remaining within expiry. | 1250 bottles |
What to do — step by step
Check Product Label
Look for the 60-count bottle labeled 'ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg)' on Amazon.
Where it went and when
Where it was distributed
Distributed in Florida.
FDA distribution: “Florida” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida.
Recall timeline
FDA terminated this recall 3 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest drug recalls
Keep exploring
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1143-2017 (June 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1143-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.