Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Finasteride Plus 1.25 mg Capsule Recalled by MasterPharm LLC Due to Cross Contamination with Other Products; Finasteride Plus 1.25mg...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact MasterPharm LLC directly.
Affected Products
Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.
Quantity: 7260 capsules
Why Was This Recalled?
Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MasterPharm LLC
MasterPharm LLC has 28 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report