CLASS I Drug recall · Reported 8 Jul 2020 · FDA Enforcement Report
Minoxidil/Biotin/Spironolactone 1.25/5 recalled by MasterPharm
MasterPharm is recalling Minoxidil/Biotin/Spironolactone 1.25/5/ per, This is a compounded drug not for resale, distributed in Florida, Maryland. The recall was initiated on 9 Jun 2020 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-1363-2020
- FDA event ID
- 85839
- Recalling firm
- MasterPharm, South Richmond Hill, NY
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 9 Jun 2020
- FDA classified
- 26 Jun 2020
- Reported
- 8 Jul 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Temperature Abuse
- Drug class
- Blood Pressure Medication
Timeline
| 9 Jun 2020 | Recall initiated by company | |
| 26 Jun 2020 | Classified by FDA | +17 days |
| 8 Jul 2020 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.
Foods that need refrigeration and were stored or shipped too warm can grow harmful bacteria without any change in look or smell.
Product as listed by the FDA
Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a compounded drug not for resale, Store at room temperature, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.
Where it was distributed
FL and MD
Questions about this recall
Why was it recalled?
Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.
Which lots are affected?
Lot #: 01-09-2020:13@8, Exp. 7/7/2020
Where was it sold?
FL and MD
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.
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|---|---|---|---|---|---|
| Drug | CLASS II | Estriol per, MasterPharm, 115-02 Liberty Ave, Richmond Hill recalled | MasterPharm | Other | Nationwide |
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| Drug | CLASS II | Tadalafil per, MasterPharm, 115-02 Liberty Ave recalled | MasterPharm | Hidden Drug Ingredients | Nationwide |
| Drug | CLASS II | Minoxidil/Biotin/Spironolactone 1.25/5/25mg capsules recalled | MasterPharm | Other | Nationwide |
| Drug | CLASS II | Tadalafil per, MasterPharm, 115-02 Liberty Ave recalled | MasterPharm | Hidden Drug Ingredients | Nationwide |