Skip to main content

MasterPharm LLC

No ongoing recalls currently shown

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.

Recalls by year
YearRecalls
202028
Download CSV

FDA Recall TerminatedTerminated: February 23, 2024Historical recordClass II

D-Biotin 300 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Published
August 5, 2020
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 23, 2024Historical recordClass II

Calcium citrate tetrahydrate USP powder, 100 gm container, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Published
August 5, 2020
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: 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.
Published
July 8, 2020
Distribution
FL and MD

View recall →

FDA Recall TerminatedTerminated: 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.
Published
May 20, 2020
Distribution
Nationwide

View recall →

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. Read the full medical disclaimer.