METHA-DROL Extreme capsules — Class I drug recall D-1151-2014
Terminated recall by Mira Health Products Ltd., reported 2014-03-12, distributed nationwide. Marketed without an Approved NDA/ANDA; product found to contain dimethazine which is a steroid and/or steroid-
| Recall number | D-1151-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mira Health Products Ltd., Farmingdale, NY, United States |
| Recall initiated | 2013-07-22 |
| Classified | 2014-03-05 |
| Reported by FDA | 2014-03-12 |
| Terminated | 2014-09-15 |
| Distributed | Nationwide (US) |
| Quantity | 5,555 bottles |
| Reason classes | unapproved product |
| Lot numbers | L54Q |
Product
METHA-DROL Extreme capsules, packaged as 60 capsules per bottle Pro-Anabolic Mass Stack Dietary Supplement, Manufactured for Blackstone Labs, Boca Raton, FL
Reason for recall
Marketed without an Approved NDA/ANDA; product found to contain dimethazine which is a steroid and/or steroid-like drug ingredient, making it an unapproved new drug
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1151-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.