Minoxidil Capsules (MasterPharm) – Superpotent Medication (2020)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
MasterPharm LLC
Lot Codes / Batch Numbers
Lot #: 01-09-2020:13@8, Exp. 7/7/2020
Products Sold
Lot #: 01-09-2020:13@8, Exp. 7/7/2020
MasterPharm LLC is recalling Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a compounded d due to Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA drug enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm, their healthcare provider, or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
FL, MD
Page updated: Jan 7, 2026