US Drug Recall Register
Class I · High risk Terminated Initiated Jun 9, 2020 (6 years ago)

Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.

What was recalled

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.

Recalling firm
MasterPharm LLC
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1363-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Iron recalls

See all