CLASS I Drug recall · Reported 12 Mar 2014 · FDA Enforcement Report
Super-DMZ Rx, Dietary Supplement, Lean muscle mass recalled
Mira Health Products is recalling Super-DMZ Rx, Dietary Supplement, Lean muscle mass, hardness and strength, distributed nationwide in the US. The recall was initiated on 22 Jul 2013 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1150-2014
- FDA event ID
- 65772
- Recalling firm
- Mira Health Products, Farmingdale, NY
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 22 Jul 2013
- FDA classified
- 5 Mar 2014
- Reported
- 12 Mar 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Hidden Drug Ingredients
Timeline
| 22 Jul 2013 | Recall initiated by company | |
| 5 Mar 2014 | Classified by FDA | +226 days |
| 12 Mar 2014 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an Approved NDA/ANDA; product contains the steroid ingredient 2, 17a-dimethyl-17b-hydroxy-5a-androst-1-en-3-one, making it an unapproved new drug
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
Super-DMZ Rx 2.0 Capsules, 60 count bottles, Dietary Supplement, Lean muscle mass, hardness and strength, Manufactured for Blackstone Labs Boca Raton, FL 33433.
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Marketed without an Approved NDA/ANDA; product contains the steroid ingredient 2, 17a-dimethyl-17b-hydroxy-5a-androst-1-en-3-one, making it an unapproved new drug
Which lots are affected?
lot numbers: 1) M55Q (A) Exp 04/2016, 2) M55Q (2) Exp 05/16, 3)E07Q Exp unknown
Where was it sold?
Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
2 other products · FDA event 65772| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | B-, Healthy Life Chemistry By Purity First recalled | Mira Health Products | Hidden Drug Ingredients | Nationwide | |
| CLASS I | Metha-drol Extreme capsules recalled by Mira Health Products | Mira Health Products | Hidden Drug Ingredients | Nationwide |
More recalls from Mira Health Products
All 83| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Metha-drol Extreme capsules recalled by Mira Health Products | Mira Health Products | Hidden Drug Ingredients | Nationwide |
| Drug | CLASS I | B-, Healthy Life Chemistry By Purity First recalled | Mira Health Products | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Bolt: Fat Incenerator capsules packaged within a container recalledBolt | Mira Health Products | Hidden Drug Ingredients | GA |
| Food | CLASS II | Biogenix USA Methadrol capsules recalled by Mira Health ProductsBiogenix USA | Mira Health Products | Undeclared Allergens | 4 states |
| Food | CLASS II | Biogenix USA HAM capsules, packaged as a bulk product recalledBiogenix USA | Mira Health Products | Undeclared Allergens | 4 states |