MasterPharm LLC

Complete recall history across all FDA and CPSC categories — 28 total recalls

MasterPharm LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Drug Recalls (28)

FDA drug safety enforcement actions by MasterPharm LLC

Date Product Reason Class
Jul 2, 2020 Estriol 8 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Vardenafil 20 mg Troche, 30 troches per bottle, MasterPharm, 115-02 Liberty A... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Tadalafil 26 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty ... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Minoxidil/Biotin/Spironolactone 1.25/5/25mg capsules, 90 capsules per bottle,... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Tadalafil 3 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty A... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Tadalafil 18 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty ... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Tadalafil 12 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty ... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 D-Biotin 300 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty ... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Calcium citrate tetrahydrate USP powder, 100 gm container, MasterPharm, 115-0... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Yohimbine HCL 5.4mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Libe... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Progesterone 300 mg Troche, 30 troches per bottle, MasterPharm, 115-02 Libert... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Sildenafil 50 mg Troche, 30 troches per bottle, MasterPharm, 115-02 Liberty A... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Formula 82F (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone Acetonide 0.01%/Finast... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Minoxidil/Biotin 1.25mg/5mg Capsule, 90 capsules per bottle, MasterPharm, 115... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Tadalafil 7 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty A... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Progesterone (Rapid-Dissolve) 150 mg Tablet, 30 tablets per bottle, MasterPha... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Progesterone (Modified Release) 150 mg Capsule, 90 capsules per bottle, Maste... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Progesterone Modified Release 100 mg Capsule, 90 capsules per bottle, MasterP... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Finasteride Plus 1.25mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 ... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Progesterone 50 mg Modified Release Capsule, 90 capsules per bottle, MasterPh... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Testosterone/Anastrozole Pellet 100/6 mg, 100 pellets per bottle, MasterPharm... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Progesterone Modified Release 200 mg Capsule, 90 capsules per bottle, MasterP... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Estriol 6 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Progesterone 200 mg Troche, 30 troches per bottle, MasterPharm, 115-02 Libert... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Progesterone 150 mg Troche, 30 troches MasterPharm, 115-02 Liberty Ave, Richm... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jul 2, 2020 Formula 82M (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone acetonide 0.01%), a) 0... Lack of Processing Controls (lack of assurance of conformity to specifications). Class II
Jun 9, 2020 Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle,... Super-potent Drug: This recall has been initiated due to the elevated presenc... Class I
Apr 14, 2020 Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Com... Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules wer... Class I

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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