MasterPharm LLC recalls Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale, MasterPhar…

Recall date

April 14, 2020

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-1269-2020

FDA classification

Class I

Brand / firm

MasterPharm LLC

Sold / distributed

Nationwide in the U.S.

Why it was recalled

Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

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.