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Based on the official records currently available to Public Health Trace, no recalls naming MasterPharm LLC are currently shown as ongoing. The 28 records below are historical recall records.
Public Health Trace has 28 recalls naming MasterPharm LLC as the recalling firm, republished from official FDA and USDA sources.
Recall history - 28 terminated records
Recalls by year
A bar chart of the number of recalls naming this company by year.
FDA RecallTerminatedTerminated: October 16, 2023Historical recordClass I
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.
by MasterPharm LLC
Reason
Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.
FDA RecallTerminatedTerminated: September 7, 2023Historical recordClass I
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.
by MasterPharm LLC
Reason
Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
Some FDA recall records on this page come from FDA's Enforcement Report database.
Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
This page lists recalls that name MasterPharm LLC as the recalling firm in the official source notice. It is
not a safety rating, ranking, or statement that the company acted negligently.
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