Recall Register

Food, drugs, devices › Firms

MasterPharm LLC

FDA recalling firm · 3 enforcement events · 28 product records · 2020–2020 · NY

MasterPharm LLC has 3 FDA enforcement events on this register (28 product records) between 2020 and 2020: 3 drug; the busiest year was 2020 with 3.

67% of its events are Class I; the most common class is Class I (2). 0 events are listed as ongoing; the recalling firm's address is in NY.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
2 Jul 2020Calcium citrate tetrahydrate USP powder, 100 gm container, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600DrugClass II26Terminated
9 Jun 2020Minoxidil/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.DrugClass I1Terminated
14 Apr 2020Finasteride 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.DrugClass I1Terminated

By type and class

Drug3
Class I2
Class II1

Class I: 67% of this firm's events; 18% of all events on the register.

Events by year

20
21
22
23
24
25
26
Enforcement events for MasterPharm LLC by year initiated.

Questions and answers

How many FDA recalls has MasterPharm LLC had?

3 enforcement events (28 product records) on this register, 2020–2020: 3 drug.

Are any MasterPharm LLC recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are MasterPharm LLC recalls?

2 Class I, 1 Class II. 67% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.